Haplogroup J-M172

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Haplogroup J-M172
J2-Y-DNA-Haplogroup-Map-J2-M172-Map-J2-Haplogrubu-Haritasi-v3.png
Possible time of origin32000 ybp [1]
Coalescence age28000 ybp [1]
Possible place of origin Upper Mesopotamia, Western Iran [2]
Ancestor J-P209
Defining mutationsM172
Highest frequencies Ingush 88.8% (Balanovsky 2011), Chechens 56.7% (Balanovsky 2011), Georgians 21% (Wells 2001)-72%, Azeris 24% (Di Giacomo 2004)-48% (Wells 2001), Iraqis 24%(Al-Zahery 2011)-25% Al-Zahery 2003 and Sanchez 2005, Cretans 35% (El-Sibai 2009), Uyghurs 34% (Shou 2010), [3] Yaghnobis 32% (Wells 2001), Uzbeks 30.4% (Shou 2010), Greeks 10%-48%(Martinez 2007), Muslim Kurds 28.4%(Nebel 2001), Lebanese 30% (Semino 2004) [ dubious – discuss ](Wells 2001), Ashkenazi Jews 24-30%(Nebel 2001) (Semino 2004), Turks 24% (Cinnioglu 2004)-40% (Semino 2000), Hazara 26.6% (Haber et al, 2012), [4] Kuwaiti 26% [ citation needed ] and (Wells 2001), Cypriots 12.9% (El-Sibai 2009)-37% (Capelli 2005), [5] Abkhaz 25% (Nasidze 2004), Iranians 22.5%(Grugni 2012)-24%, [6] Balkars 24% (Battaglia 2008), Italians 9%-36%(Capelli 2007) and (Semino 2000), Armenians 21%(Wells 2001)-24% (Nasidze 2004), Palestinians 29%(Nebel 2001)[ citation needed ], Mordvins 15.3%, [7] Kazan Tatars 15.1%, [7] Chuvash 14%, [7] Sephardi Jews 15 -20% (Shen 2004)-29% (Nebel 2001), Ossetians 16%(Balanovsky 2011)-24%(Nasidze 2004), Circassians 21.8% (Balanovsky 2011), Maltese 21% (Capelli 2005), Lemba 20.8% (Soodyall 2013), North Indian Shia Muslims 18% (Eaaswarkhanth 2009), Albanians 16% (Battaglia 2008), Syrians 14% (Di Giacomo 2004)-29%[ citation needed ], and Kalash people 9.1%.(Firasat 2007) [8]

In human genetics, Haplogroup J-M172 or J2 [Phylogenetics 1] is a Y-chromosome haplogroup which is a subclade (branch) of haplogroup J-M304. [Phylogenetics 2] Haplogroup J-M172 is common in modern populations in Western Asia, Central Asia, South Asia, Southern Europe, Northwestern Iran and North Africa. It is thought that J-M172 may have originated between the Caucasus, Anatolia and/or Western Iran. [9] [10]

Contents

It is further divided into two complementary clades, J-M410 and J-M12 (M12, M102, M221, M314).

Origins

The date of origin for haplogroup J-M172 was estimated by Batini et al in 2015 as between 19,000 and 24,000 years before present (BP). [11] Samino et al in 2004 dated the origin of the parent haplogroup, J-P209, to between 18,900 and 44,500 YBP. [12] Ancient J-M410, specifically subclade J-Y12379*, has been found, in a mesolithic context, in a tooth from the Kotias Klde Cave in western Georgia dating 9.529-9.895 cal. BP. [13] This sample has been assigned to the Caucasus hunter-gatherers (CHG) autosomal component. [14] J-M410, more specifically its subclade J-PF5008, has also been found in a mesolithic sample from the Hotu and Kamarband Caves located in Mazandaran Province of Iran, dating back to 9,100-8,600 B.C.E (approximately 11,000 ybp). [15] Both samples belong to the Trialetian Culture. It is likely that J2 men had settled over most of Anatolia, the South Caucasus and the Zagros mountains by the end of the Last Glaciation 12,000 years ago. [16]

Zalloua and Wells 2004 and al-Zaheri 2003 claimed to have uncovered the earliest known migration of J2, expanded possibly from Anatolia and the Caucasus. [9] [10] [17] In 2001, Nebel et al. found that, "According to Underhill et al. (2000), Eu 9 (H58) evolved from Eu 10 (H71) through a T→G transversion at M172 (emphasis added)," and that in today's populations, Eu 9 (the post-mutation form of M172) is strongest in the Caucasus, Asia Minor and the Levant, whilst Eu 10 becomes stronger and replaces the frequency of Eu 9 as one moves south into the Arabian Peninsula, [18] so that people from the Caucasus met with Arabs near and between Mesopotamia (Sumer/Assyria) and the Negev Desert, as "Arabisation" spread from Arabia to the Fertile Crescent and Turkey.

Per research by Di Giacomo 2004, J-M172 haplogroup spread into Southern Europe from either the Levant or Anatolia, likely parallel to the development of agriculture. [19] As to the timing of its spread into Europe, Di Giacomo points to events which post-date the Neolithic, in particular the demographic floruit associated with the rise of the Ancient Greek world. Semino et al. derived older age estimates for overall J2 (having used the Zhivotovsky method c.f. Di Giacomo), postulating its initial spread with Neolithic farmers from the Near East. However, its subclade distribution, showing localized peaks in the Southern Balkans, southern Italy, north/central Italy and the Caucasus, does not conform to a single 'wave-of-advance' scenario, betraying a number of still poorly understood post-Neolithic processes which created its current pattern. Like Di Giacomo, the Bronze Age southern Balkans was suggested by Semino 2004 to have been an important vector of spread. [12]

Distribution

Haplogroup J-M172 is found mainly in the Fertile Crescent, the Caucasus ( Nasidze 2003 ), Anatolia, Italy, the Mediterranean littoral, and the Iranian plateau ( Semino 2004 ). Y-DNA: J2 (J-M172): Syrid/Nahrainid Arabid(s).

The highest reported frequency of J-M172 ever was 87.4%, among Ingush in Malgobek ( Balanovsky 2011 ).

More specifically it is found in Iraq ( Al-Zahery 2003 ), Kuwait, [20] Syria ( Luis 2004 ), Lebanon ( Zalloua 2008l ), Turkey ( Cinnioglu 2004 ), Georgia ( Nasidze 2003 ), Azerbaijan ( Di Giacomo 2004 ), North Caucasus ( Nasidze 2004 ), Armenia ( Wells 2001 ), Iran ( Nasidze 2004 ), Israel ( Semino 2004 ), Palestine ( Semino 2004 ), Cyprus ( Capelli 2005 ), Greece ( Martinez 2007 ), Albania ( Semino 2000 ), Italy ( Capelli 2007 ), Spain ( Di Giacomo 2003 ), and more frequently in Iraqis 24% ( Al-Zahery 2011 ), Chechens 51.0%-58.0% ( Balanovsky 2011 ), Georgians 21% ( Wells 2001 )-72% ( Wells 2001 ), Lebanese 30% ( Semino 2004 ), Ossetians 24% ( Nasidze 2004 ), Balkars 24% ( Battaglia 2008 ), Syrians 23% ( Luis 2004 ), Turks 13% ( Cinnioglu 2004 )-40% ( Semino 2000 ), Cypriots 12.9% ( El-Sibai 2009 )-37% ( Capelli 2005 ), Armenians 21% ( Wells 2001 )-24% ( Nasidze 2004 ), Circassians 21.8%( Balanovsky 2011 ), Iranians 10% ( Nasidze 2004 )-25% ( Wells 2001 ), Albanians 16% ( Battaglia 2008 ) and ( Semino 2000 ), Italians 9%-36% ( Capelli 2007 ), Sephardi Jews 15% ( Nebel 2001 )-29%( Semino 2004 ), Maltese 21% ( Capelli 2005 ), Palestinians 17% ( Semino 2004 ), Saudis 14% ( Abu-Amero 2009 ), Jordanians 14%, Omanis 10%-15% ( Di Giacomo 2004 ) and ( Luis 2004 ) and North Indian Shia Muslim 18% ( Eaaswarkhanth 2009 ).

North Africa

Haplogroup J2 is found with low frequencies in North Africa. with a hotspot in Sousse region Fadhlaoui-Zid 2014 most of Sousse samples have the same haplotypes found in Haplogroup J-L271 which was found in Msaken.

Country/RegionSamplingNJ-M172Study
TunisiaTunisia628 El-Sibai 2009
TunisiaSousse2208.2 Fadhlaoui-Zid 2014
AlgeriaOran1024.9 Robino 2008
Egypt1247.6 El-Sibai 2009
Egypt14712.0 Abu-Amero 2009
Morocco2214.1 Fregel 2009
North AfricaAlgeria, Tunisia2023.5 Fregel 2009

Central Asia

Country/RegionSamplingNJ-M172Study
XinjiangLop Uyghurs6457.8 Liu 2018
XinjiangUyghurs5034 Shou 2010
TajikistanYaghnobis3132 Wells 2001
DushanbeTajiks1631 Wells 2001
XinjiangUzbeks2330.4 Shou 2010
AfghanistanHazara6026.6 Haber 2012
XinjiangKeriyan Uyghurs3925.6 Liu 2018
KazakhstanUyghurs4120 Wells 2001
SamarkandTajiks4020 Wells 2001
TajikistanTajiks3818.4 Wells 2001
TurkmenistanTurkmens3017 Wells 2001
XinjiangPamiri Tajiks3116.1 Shou 2010
AfghanistanUzbeks12616 Di Cristofaro 2013
BukharaUzbeks5816 Wells 2001
SamarkandUzbeks4516 Wells 2001
SurkhandaryaUzbeks6816 Wells 2001
UzbekistanUzbeks36613.4 Wells 2001
KazakhstanKazakhs3013.3 Karafet 2001
Turpan areaUyghurs1439.8[ citation needed ]
Hotan areaUyghurs4789.2[ citation needed ]
ChangjiHui1759.1[ citation needed ]
XinjiangDolan Uyghurs767.9 Liu 2018
NingxiaHui657.7[ citation needed ]
Kizilsu Kyrgyz 2416.64% Guo 2020
Kazakhstan Kazakhs 12944.33% Ashirbekov 2017
Kyrgyzstan Kyrgyz 1323.79% Di Cristofaro 2013

J-M172 is found at moderate frequencies among Central Asian people such as Uyghurs, Uzbeks, Turkmens, Tajiks, Kazakhs, and Yaghnobis. According to the genetic study in Northwest China by Shou et al. (2010), a notable high frequency of J-M172 is observed particularly in Uyghurs 34% and Uzbeks 30.4% in Xinjiang, China. Liu Shuhu et al. (2018) found J2a1 (L26/Page55/PF5110/S57, L27/PF5111/S396) in 43.75% (28/64) and J2a2 (L581/S398) in 14.06% (9/64) of a sample of Lop Uyghurs from Qarchugha Village of Yuli (Lopnur) County, Xinjiang, J2a1b1 (M92, M260/Page14) in 25.64% (10/39) of a sample of Keriyan Uyghurs from Darya Boyi Village of Yutian (Keriya) County, Xinjiang, and J2a1 (L26/Page55/PF5110/S57, L27/PF5111/S396) in 3.95% (3/76) and J2a2 (L581/S398) in 3.95% (3/76) of a sample of Dolan Uyghurs from Horiqol Township of Awat County, Xinjiang. [21] Only far northwestern ethnic minorities had haplogroup J in Xinjiang, China. Uzbeks in the sample had 30.4% J2-M172 and Tajiks of Xinjiang and Uyghurs also had it. [22]

The haplogroup has an ancient presence in Central Asia and seems to have preceded the spread of Islam ( Shou 2010 ). In addition, the immediate ancestor of J-M172, namely J* (J-M304*, a.k.a. J-P209*, J-12f2.1*) is also found among Xibo, Kazakh, Dongxiang and Uzbek people in Northwest China.

In 2015, two ancient samples belonging to J-M172 or J-M410 (J2a) were found at two different archaeological sites in Altai, eastern Russia: Kytmanovo and Sary-bel kurgan. Both of the ancient samples are related to Iron Age cultures in Altai. Sary-bel J2/J2a is dated to 50 BC whereas Kytmanovo sample is dated to 721-889 AD. Genetic admixture analysis of these samples also suggests that the individuals were more closely related to West Eurasians than other Altaians from the same period, although they also seem to be related to present-day Turkic peoples of the region. [23] [24] [25]

Europe

Country/RegionSamplingNJ-M172Study
Albania5519.9%
11/55		Battaglia 2009
Bosnia-HerzegovinaSerbs818.7Battaglia 2009
Cyprus16412.9 El-Sibai 2009
GreeceCrete14335 El-Sibai 2009
Iberia6557 Fregel 2009
Iberia11407.7 Adams 2008
ItalySicily21222.6 El-Sibai 2009
ItalyMainland69920 Capelli 2007
ItalyCentral Marche5935.6 Capelli 2007
ItalyWest Calabria5735.1 Capelli 2007
ItalyVal Badia348.8 Capelli 2007
Malta9021.1 El-Sibai 2009
PortugalNorth, Center, South3036.9 El-Sibai 2009
PortugalTras-os-Montes (Jews)5724.5 Nogueiro 2010
Sardinia819.9 El-Sibai 2009
SpainMallorca628.1 El-Sibai 2009
SpainSevilla1557.8 El-Sibai 2009
SpainLeon605 El-Sibai 2009
SpainIbiza543.7 El-Sibai 2009
SpainCantabria702.9 El-Sibai 2009
SpainGalicia29213[ citation needed ]
SpainCanary Islands65210.5 Fregel 2009

In Europe, the frequency of Haplogroup J-M172 drops as one moves northward away from the Mediterranean. In Italy, J-M172 is found with regional frequencies ranging between 9% and 36% ( Capelli 2007 ). In Greece, it is found with regional frequencies ranging between 10% and 48%. Approximately 24% of Turkish men are J-M172 according to a recent study, ( Cinnioglu 2004 ) with regional frequencies ranging between 13% and 40% ( Semino 2000 ). Combined with J-M267, up to half of the Turkish population belongs to Haplogroup J-P209.

It has been proposed that haplogroup subclade J-M410 was linked to populations on ancient Crete by examining the relationship between Anatolian, Cretan, and Greek populations from around early Neolithic sites in Crete. Haplogroup J-M172 was associated with Neolithic Greece (ca. 8500 - 4300 BCE) and was reported to be found in modern Crete (3.1%) and mainland Greece (Macedonia 7.0%, Thessaly 8.8%, Argolis 1.8%) ( King 2008 ).

North Caucasus

Country/RegionSamplingNJ-M172Study
CaucasusAbkhaz5813.8 Balanovsky 2011
CaucasusAvar1156 Balanovsky 2011
CaucasusChechen33057 Balanovsky 2011
CaucasusAdyghe14221.8 Balanovsky 2011
CaucasusDargins1011 Balanovsky 2011
CaucasusIngush14388.8 Balanovsky 2011
CaucasusKaitak333 Balanovsky 2011
CaucasusKumyks7321 Yunusbayev 2012
CaucasusKubachi650 Balanovsky 2011
CaucasusLezghins812.5 Balanovsky 2011
CaucasusOssets35716 Balanovsky 2011
CaucasusShapsug1006 Balanovsky 2011
Caucasus152528.1 Balanovsky 2011

J-M172 is found at very high frequencies in certain peoples of the Caucasus: among the Ingush 87.4% ( Balanovsky 2011 ), Chechens 55.2% ( Balanovsky 2011 ), Georgians 21%-72%, ( Wells 2001 ), Azeris 24% ( Di Giacomo 2004 )-48%, ( Wells 2001 ) Abkhaz 25%, ( Nasidze 2004 ) Balkars 24% ( Battaglia 2008 ), Ossetians 24% ( Nasidze 2004 ), Armenians 21% ( Wells 2001 )-24% ( Nasidze 2004 ), Adyghe 21.8% ( Balanovsky 2011 ), and other groups ( Nasidze 2004 and Nasidze 2003).

West Asia

Country/RegionSamplingNJ-M172Study
JewishAshkenazim Jewish44219 Behar 2004
Iran9225 El-Sibai 2009
Iraq15424 Al-Zahery 2011 [26]
Palestinian ArabAkka10118.6 El-Sibai 2009
Jordan27314.6 El-Sibai 2009
Lebanon95129.4 El-Sibai 2009
Oman12110.0 Abu-Amero 2009
Qatar728.3 El-Sibai 2009
Saudi Arabia15714 Abu-Amero 2009 [27]
SyriaSyria55420.8 El-Sibai 2009
Turkey52324.2 El-Sibai 2009
UAE16410.3 El-Sibai 2009
Yemen629.6 El-Sibai 2009

Sephardi Jews have about 15% ( Nebel 2001 )-29% ( Semino 2004 ), of haplogroup J-M172, and Ashkenazi Jews have 15% ( Shen 2004 )-23% ( Semino 2004 ). It was reported in an early study which tested only four STR markers ( Malaspina 2001 ) that a small sample of Italian Cohens belonged to Network 1.2, an early designation for the overall clade now known as J-L26, defined by the deletion at DYS413. However, a large number of all Jewish Cohens in the world belong to haplogroup J-M267 (see Cohen modal haplotype).

Haplogroup J-M172 has been shown to have a more northern distribution in the Middle East, although it exists in significant amounts in the southern middle-east regions, a lesser amount of it was found when compared to its brother haplogroup, J-M267, which has a high frequency southerly distribution. It was believed that the source population of J-M172 originated from the Levant/Syria (Syrid-J-M172), and that its occurrence among modern populations of Europe, Central Asia, and South Asia was a sign of the neolithic agriculturalists. However, as stated it is now believed more likely to have been spread in waves, as a result of post-Neolithic processes .

South Asia

Haplogroup J2 has been present in South Asia mostly as J2a-M410 and J2b-M102, since neolithic times (9500 YBP). [28] [29] J2-M172 was found to be significantly higher among Dravidian castes at 19% than among Indo-Aryan castes at 11%. J2-M172 and J-M410 is found 21% among Dravidian middle castes, followed by upper castes, 18.6%, and lower castes 14%. [30] Among caste groups, the highest frequency of J2-M172 was observed among Tamil Vellalars of South India, at 38.7%. [30] J2 is present in Indian tribals too and has a frequency of 11% in Austro-Asiatic tribals. Among the Austro-Asiatic tribals, the predominant J2 occurs in the Asur tribe (77.5%) albeit with a sample size of 40 [28] and in the Lodha (35%) of West Bengal. [30] J2 is also present in the South Indian hill tribe Toda at 38.46% albeit with a sample size of only 26, [31] in the Andh tribe of Telangana at 35.19%, [32] in the Narikuravar tribe at 57.9% [28] and in the Kol tribe of Uttar Pradesh at a frequency of 33.34%. [33] Haplogroup J-P209 was found to be more common in India's Shia Muslims, of which 28.7% belong to haplogroup J, with 13.7% in J-M410, 10.6% in J-M267 and 4.4% in J2b ( Eaaswarkhanth 2009 ).

In Pakistan, the highest frequencies of J2-M172 were observed among the Parsis at 38.89%, the Dravidian speaking Brahui's at 28.18% and the Makrani Balochs at 24%. [34] It also occurs at 18.18% in Makrani Siddis and at 3% in Karnataka Siddis. [34] [35]

J2-M172 is found at an overall frequency of 16.1% in the people of Sri Lanka. [36] In Maldives, 22% of Maldivian population were found to be haplogroup J2 positive. [37] Subclades of M172 such as M67 and M92 were not found in either Indian or Pakistani samples which also might hint at a partial common origin. [30]

J2-M172 has been observed in 15.9% (20/164 J2a-M410, 6/164 J2b2-M241) of Tharu from Uttar Pradesh, [38] 13.4% (19/202 J2a-M410, 8/202 J2b2-M241) of Tharu from Nepal, [39] [38] and 8.9% (4/45 J2a-M410) of Tharu from Uttarakhand. [38]

Subclade distribution

Haplogroup J-M172 is subdivided into two complementary sub-haplogroups: J-M410, defined by the M410 genetic marker, and J-M12, defined by the M12 genetic marker.

J-M172

J-M172 is typical of populations of the Near East, Southern Europe, Southwest Asia and the Caucasus, with a moderate distribution through much of Central Asia, South Asia, and North Africa. [40]

J-M410

J-M410* is found in Georgia, North Ossetia. [41]

J-M47

J-M47 is found with low frequency in Georgia, ( Battaglia 2008 ) southern Iran ( Regueiro 2006 ), Qatar ( Cadenas 2008 ) Saudi Arabia ( Abu-Amero 2009 ), Syria ( Di Giacomo 2004 ), Tunisia ( Arredi 2004 ), Turkey (Di Giacomo 2004 and Cinnioglu 2004), the UAE, ( Cadenas 2008 ), and Central Asia/Siberia ( Underhill 2000 ).

J-M67

J-M67 (called J2f in older papers) has its highest frequencies associated with Nakh peoples. Found at very high (majority) frequencies among Ingush in Malgobek (87.4%), Chechens in Dagestan (58%), Chechens in Chechnya (56.8%) and Chechens in Malgobek, Ingushetia (50.9%) ( Balanovsky 2011 ). In the Caucasus, it is found at significant frequencies among Georgians (13.3%) ( Semino 2004 ), Iron Ossetes (11.3%), South Caucasian Balkars (6.3%) ( Semino 2004 ), Digor Ossetes (5.5%), Abkhaz (6.9%), and Cherkess (5.6%) ( Balanovsky 2011 ). It is also found at notable frequencies in the Mediterranean and Middle East, including Cretans (10.2%), North-central Italians (9.6%), Southern Italians (4.2%; only 0.8% among N. Italians), Anatolian Turks (2.7-5.4%), Greeks (4-4.3%), Albanians (3.6%), Ashkenazi Jews (4.9%), Sephardis (2.4%), Catalans (3.9%), Andalusians (3.2%), Calabrians (3.3%), Albanian Calabrians (8.9%) (see Di Giacomo 2004 and Semino 2004).

J-M92/M260, a subclade of J-M67, has been observed in 25.64% (10/39) of a sample of Keriyan Uyghurs from Darya Boyi Village of Yutian (Keriya) County, Xinjiang. [21] This Uyghur village is located in a remote oasis in the Taklamakan Desert.

J-M319

J-M319 is found with low to moderate frequency in Cretan Greeks (Martinez 2007 and King 2008), Iraqi Jews ( Shen 2004 ), and Moroccan Jews ( Shen 2004 ).

J-M158

J-M158 (location under L24 uncertain) J-M158 is found with low frequency in Turkey ( Cinnioglu 2004 ), South Asia (Sengupta 2006 and Underhill 2000), Indochina ( Underhill 2000 ), and Iberian Peninsula.

Phylogenetics

In Y-chromosome phylogenetics, subclades are the branches of haplogroups. These subclades are also defined by single nucleotide polymorphisms (SNPs) or unique event polymorphisms (UEPs).

Phylogenetic history

Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.

YCC 2002/2008 (Shorthand)(α)(β)(γ)(δ)(ε)(ζ)(η)YCC 2002 (Longhand)YCC 2005 (Longhand)YCC 2008 (Longhand)YCC 2010r (Longhand)ISOGG 2006ISOGG 2007ISOGG 2008ISOGG 2009ISOGG 2010ISOGG 2011ISOGG 2012
J-12f2a 9VIMed23Eu10H4BJ*JJJ------J
J-M62 9VIMed23Eu10H4BJ1J1aJ1aJ1a------Private
J-M1729VIMed24Eu9H4BJ2*J2J2J2------J2
J-M47 9VIMed24Eu9H4BJ2aJ2aJ2a1J2a4a------J2a1a
J-M68 9VIMed24Eu9H4BJ2bJ2bJ2a3J2a4c------J2a1c
J-M137 9VIMed24Eu9H4BJ2cJ2cJ2a4J2a4h2a1------J2a1h2a1a
J-M158 9VIMed24Eu9H4BJ2dJ2dJ2a5J2a4h1------J2a1h1
J-M12 9VIMed24Eu9H4BJ2e*J2eJ2bJ2b------J2b
J-M102 9VIMed24Eu9H4BJ2e1*J2e1J2bJ2b------J2b
J-M99 9VIMed24Eu9H4BJ2e1aJ2e1aJ2b2aJ2b2a------Private
J-M67 9VIMed24Eu9H4BJ2f*J2fJ2a2J2a4b------J2a1b
J-M92 9VIMed24Eu9H4BJ2f1J2f1J2a2aJ2a4b1------J2a1b1
J-M163 9VIMed24Eu9H4BJ2f2J2f2J2a2bJ2a4b2------Private

Research publications

The following research teams per their publications were represented in the creation of the YCC Tree.

Phylogenetic trees

There are several confirmed and proposed phylogenetic trees available for haplogroup J-M172. The scientifically accepted one is the Y-Chromosome Consortium (YCC) one published in Karafet 2008 and subsequently updated. A draft tree that shows emerging science is provided by Thomas Krahn at the Genomic Research Center in Houston, Texas. The International Society of Genetic Genealogy (ISOGG) also provides an amateur tree. [Phylogenetics 3] [42]

The Genomic Research Center draft tree

This is Thomas Krahn at the Genomic Research Center's draft tree Proposed Tree for haplogroup J-M172 ( Krahn & FTDNA 2013 ). For brevity, only the first three levels of subclades are shown.

  • M172, L228
    • M410, L152, L212, L505, L532, L559
      • PF5008
        • Y182822
          • L581
            • Z37823
      • PF4610
        • Z6046
        • L26
    • M12, M102, M221, M314, L282
      • M205
      • M241
        • M99
        • M280
        • M321
        • P84
        • L283

The Y-Chromosome Consortium tree

This is the official scientific tree produced by the Y-Chromosome Consortium (YCC). The last major update was in 2008 ( Karafet 2008 ). Subsequent updates have been quarterly and biannual. The current version is a revision of the 2010 update. [43]

The ISOGG tree

Below are the subclades of Haplogroup J-M172 with their defining mutation, according to the ISOGG tree (as of January 2020). Note that the descent-based identifiers may be subject to change, as new SNPs are discovered that augment and further refine the tree. For brevity, only the first three levels of subclades are shown.

  • J2 M172/Page28/PF4908, L228/PF4895/S321
    • J2a M410, L152, L212/PF4988, L559/PF4986
      • J2a1 DYS413≤18, L26/Page55/PF5110/S57, F4326/L27/PF5111/S396
        • J2a1a M47, M322
        • J2a1b M67/PF5137/S51
        • J2a1c M68
        • J2a1d M319
        • J2a1e M339
        • J2a1f M419
        • J2a1g P81/PF4275
        • J2a1h L24/S286, L207.1
        • J2a1i L88.2, L198
      • J2a2 L581/PF5026/S398
        • J2a2a P279/PF5065
    • J2b M12
      • J2b1 M205
        • J2b1a~ A11525, PH4306, Y22059, Y22060, Y22061, Y22062, Y22063
        • J2b1b~ CTS1969
      • J2b2~ CTS2622/Z1827, CTS11335/Z2440, Z575
        • J2b2a M241

See also

Genetics

Other Y-DNA J Subclades

Y-DNA Backbone Tree

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Haplogroup J-M304, also known as J, is a human Y-chromosome DNA haplogroup. It is believed to have evolved in Western Asia. The clade spread from there during the Neolithic, primarily into North Africa, the Horn of Africa, the Socotra Archipelago, the Caucasus, Europe, Anatolia, Central Asia, South Asia, and Southeast Asia.

E-M215, also known as E1b1b-M215, is a human Y-chromosome DNA haplogroup. E-M215 has two basal branches, E-M35 and E-M281. E-M35 is primarily distributed in North Africa and the Horn of Africa, and occurs at lower frequencies in the Middle East, Europe, and Southern Africa. E-M281 occurs at a low frequency in Ethiopia.

Haplogroup E-M96 is a human Y-chromosome DNA haplogroup. It is one of the two main branches of the older and ancestral haplogroup DE, the other main branch being haplogroup D. The E-M96 clade is divided into two main subclades: the more common E-P147, and the less common E-M75.

<span class="mw-page-title-main">Haplogroup L-M20</span> Human Y chromosome DNA grouping common in South Asia and the Mediterranean

Haplogroup L-M20 is a human Y-DNA haplogroup, which is defined by SNPs M11, M20, M61 and M185. As a secondary descendant of haplogroup K and a primary branch of haplogroup LT, haplogroup L currently has the alternative phylogenetic name of K1a, and is a sibling of haplogroup T.

Haplogroup P also known as P-F5850 or K2b2 is a Y-chromosome DNA haplogroup in human genetics. P-F5850 is a branch of K2b, which is a branch of Haplogroup K2 (K-M526).

<span class="mw-page-title-main">Human Y-chromosome DNA haplogroup</span> Human DNA groupings

In human genetics, a human Y-chromosome DNA haplogroup is a haplogroup defined by mutations in the non-recombining portions of DNA from the male-specific Y chromosome. Many people within a haplogroup share similar numbers of short tandem repeats (STRs) and types of mutations called single-nucleotide polymorphisms (SNPs).

<span class="mw-page-title-main">Haplogroup J-M267</span> Human Y-chromosome DNA haplogroup

Haplogroup J-M267, also commonly known as Haplogroup J1, is a subclade (branch) of Y-DNA haplogroup J-P209 along with its sibling clade haplogroup J-M172.

The various ethnolinguistic groups found in the Caucasus, Central Asia, Europe, the Middle East, North Africa and/or South Asia demonstrate differing rates of particular Y-DNA haplogroups.

Haplogroup E-M132, formerly known as E-M33 (E1a), is a human Y-chromosome DNA haplogroup. Along with E-P177, it is one of the two main branches of the older E-P147 paternal clade. E-M132 is divided into two primary sub-branches, E-M44 and E-Z958, with many descendant subclades.

Haplogroup E-M75 is a human Y-chromosome DNA haplogroup. Along with haplogroup E-P147, it is one of the two main branches of the older haplogroup E-M96.

Haplogroup E-V68, also known as E1b1b1a, is a major human Y-chromosome DNA haplogroup found in North Africa, the Horn of Africa, Western Asia and Europe. It is a subclade of the larger and older haplogroup, known as E1b1b or E-M215. The E1b1b1a lineage is identified by the presence of a single nucleotide polymorphism (SNP) mutation on the Y chromosome, which is known as V68. It is a subject of discussion and study in genetics as well as genetic genealogy, archaeology, and historical linguistics.

Haplogroup E-P2, also known as E1b1, is a human Y-chromosome DNA haplogroup. E-P2 has two basal branches, E-V38 and E-M215. E-P2 had an ancient presence in East Africa and the Levant; presently, it is primarily distributed in Africa where it may have originated, and occurs at lower frequencies in the Middle East and Europe.

Y-DNA haplogroups in populations of Europe are haplogroups of the male Y-chromosome found in European populations.

Listed here are notable ethnic groups and populations from Western Asia, Egypt and South Caucasus by human Y-chromosome DNA haplogroups based on relevant studies. The samples are taken from individuals identified with the ethnic and linguistic designations in the first two columns, the third column gives the sample size studied, and the other columns give the percentage of the particular haplogroup. Some old studies conducted in the early 2000s regarded several haplogroups as one haplogroup, e.g. I, G and sometimes J were haplogroup 2, so conversion sometimes may lead to unsubstantial frequencies below.

Various Y-DNA haplogroups have differing frequencies within each ethnolinguistic group in the Caucasus region.

Haplogroup Q-M25, also known as Q1a1b is a subclade or branch of human Y-DNA haplogroup Q-F1096 (Q1a1), which is, in turn, a subclade of Q-MEH2 (Q1a). In human genetics, each Y-DNA haplogroup constitutes a biological paternal lineages back to a shared common male ancestor.

<span class="mw-page-title-main">Haplogroup R-M269</span> Gene group

Haplogroup R-M269 is the sub-clade of human Y-chromosome haplogroup R1b that is defined by the SNP marker M269. According to ISOGG 2020 it is phylogenetically classified as R1b1a1b. It underwent intensive research and was previously classified as R1b1a2, R1b1c, R1b1b2 and R1b1a1a2.

<span class="mw-page-title-main">Haplogroup E-M329</span> Human Y-chromosome DNA haplogroup

Haplogroup E-M329, also known as E1b1a2, is a human Y-chromosome DNA haplogroup. E-M329 is mostly found in East Africa.

References

  1. 1 2 "YFull YTree v7.05.00". yfull.com. Archived from the original on 2019-06-18. Retrieved 2019-09-27.
  2. ↑ The extent of differentiation of Hg J, observed both with the biallelic and microsatellite markers, points to the Middle East as its likely homeland. In this area, J-M172 and J-M267 are equally represented and show the highest degree of internal variation, indicating that it is most likely that these subclades also arose in the Middle East. (Di Giacomo 2004)
  3. ↑ Shou, Wei-Hua; Qiao, En-Fa; Wei, Chuan-Yu; Dong, Yong-Li; Tan, Si-Jie; Shi, Hong; Tang, Wen-Ru; Xiao, Chun-Jie (2010). "Y-chromosome distributions among populations in Northwest China identify significant contribution from Central Asian pastoralists and lesser influence of western Eurasians". Journal of Human Genetics. 55 (5): 314–322. doi: 10.1038/jhg.2010.30 . PMID   20414255.
  4. ↑ Haber M, Platt DE, Ashrafian Bonab M, Youhanna SC, Soria-Hernanz DF, Martínez-Cruz B, et al. (2012). "Afghanistan's ethnic groups share a Y-chromosomal heritage structured by historical events". PLOS ONE. 7 (3): e34288. Bibcode:2012PLoSO...734288H. doi: 10.1371/journal.pone.0034288 . PMC   3314501 . PMID   22470552.
  5. ↑ Capelli C, Redhead N, Romano V, Cali F, Lefranc G, Delague V, et al. (2006). "Population Structure in the Mediterranean Basin: A Y Chromosome Perspective". Annals of Human Genetics. 70 (2): 207–225. doi: 10.1111/j.1529-8817.2005.00224.x . hdl: 2108/37090 . PMID   16626331. S2CID   25536759.
  6. ↑ "Y haplogroup J in Iran by Alfred A. Aburto Jr". Archived from the original on 2012-10-13. Retrieved 2014-04-06.
  7. 1 2 3 "Трофимова Наталья Вадимовна, ИЗМЕНЧИВОСТЬ МИТОХОНДРИАЛЬНОЙ ДНК И Y-ХРОМОСОМЫВ ПОПУЛЯЦИЯХ ВОЛГО-УРАЛЬСКОГО РЕГИОНА, 03.02.07" (PDF). Archived from the original (PDF) on 2015-01-14. Retrieved 2015-01-07.
  8. ↑ A genetic study published led by Firasat (2007) on Kalash individuals found high and diverse frequencies.
  9. 1 2 Zalloua & Wells: National Geographic Magazine, October 2004. Archived 2014-04-07 at the Wayback Machine and Archived 2012-02-10 at the Wayback Machine .
  10. 1 2 "N. Al-Zahery et al. "Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migrations" (2003)" (PDF). Family Tree DNA. Archived from the original (PDF) on 27 December 2010. Retrieved 1 September 2013.
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  12. 1 2 Semino O, Magri C, Benuzzi G, Lin AA, Al-Zahery N, Battaglia V, et al. (May 2004). "Origin, Diffusion, and Differentiation of Y-Chromosome Haplogroups E and J: Inferences on the Neolithization of Europe and Later Migratory Events in the Mediterranean Area". American Journal of Human Genetics. 74 (5): 1023–34. doi:10.1086/386295. PMC   1181965 . PMID   15069642.
  13. ↑ "[Homepage]". YFull. Archived from the original on 2020-04-23. Retrieved 2020-05-11.
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  15. ↑ Lazaridis, Iosif; Nadel, Dani; Rollefson, Gary; Merrett, Deborah C.; Rohland, Nadin; Mallick, Swapan; Fernandes, Daniel; Novak, Mario; Gamarra, Beatriz; Sirak, Kendra; Connell, Sarah; Stewardson, Kristin; Harney, Eadaoin; Fu, Qiaomei; Gonzalez-Fortes, Gloria; Jones, Eppie R.; Roodenberg, Songül Alpaslan; Lengyel, György; Bocquentin, Fanny; Gasparian, Boris; Monge, Janet M.; Gregg, Michael; Eshed, Vered; Mizrahi, Ahuva-Sivan; Meiklejohn, Christopher; Gerritsen, Fokke; Bejenaru, Luminita; Blüher, Matthias; Campbell, Archie; Cavalleri, Gianpiero; Comas, David; Froguel, Philippe; Gilbert, Edmund; Kerr, Shona M.; Kovacs, Peter; Krause, Johannes; McGettigan, Darren; Merrigan, Michael; Merriwether, D. Andrew; O'Reilly, Seamus; Richards, Martin B.; Semino, Ornella; Shamoon-Pour, Michel; Stefanescu, Gheorghe; Stumvoll, Michael; Tönjes, Anke; Torroni, Antonio; Wilson, James F.; Yengo, Loic; Hovhannisyan, Nelli A.; Patterson, Nick; Pinhasi, Ron; Reich, David (August 2016). "Genomic insights into the origin of farming in the ancient Near East". Nature. 536 (7617): 419–424. Bibcode:2016Natur.536..419L. doi:10.1038/nature19310. PMC   5003663 . PMID   27459054.
  16. ↑ "The spread of the bull". Cradle of Civilization. 2018-07-15. Retrieved 2023-10-21.
  17. ↑ Al-Zahery, N. (2003). "Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migrations". Molecular Phylogenetics and Evolution. 28 (3): 458–72. doi:10.1016/s1055-7903(03)00039-3. PMID   12927131.
  18. ↑ Nebel A, Filon D, Brinkmann B, Majumder PP, Faerman M, Oppenheim A (Nov 2001). "The Y Chromosome Pool of Jews as Part of the Genetic Landscape of the Middle East". American Journal of Human Genetics. 69 (5): 1095–1112. doi:10.1086/324070. PMC   1274378 . PMID   11573163.See especially Figure Six.Semino 2000 is a source which also states that Eu 9 descends from Eu 10 (Eu 10 is a different subclade of Haplogroup J (mtDNA)).
  19. ↑ Di Giacomo F, Luca F, Popa LO, Akar N, Anagnou N, Banyko J, et al. (2004). "Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe". Human Genetics. 115 (5): 357–71. doi:10.1007/s00439-004-1168-9. PMID   15322918. S2CID   18482536.
  20. ↑ Al-Zahery, N.; Semino, O.; Benuzzi, G.; Magri, C.; Passarino, G.; Torroni, A.; Santachiara-Benerecetti, A. S. (2003-09-01). "Y-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migrations". Molecular Phylogenetics and Evolution. Special Issue: Papers presented at the Mammalian Phylogeny symposium during the 2002 Annual Meeting of the Society for Molecular Biology and Evolution, Sorrento, Italy, June 13–16, 2002. 28 (3): 458–472. doi:10.1016/S1055-7903(03)00039-3. ISSN   1055-7903.
  21. 1 2 Liu Shuhu; Nizam Yilihamu; Rabiyamu Bake; Abdukeram Bupatima; Dolkun Matyusup (2018). "Yìngyòng Y rǎnsètǐ SNP duì Xīnjiāng sān gè gélí rénqún yíchuán duōyàng xìng de yánjiū" 应用 Y 染色体 SNP 对新疆三个隔离人群遗传多样性的研究 [A study of genetic diversity of three isolated populations in Xinjiang using Y-SNP]. Rénlèixué xuébào / Acta Anthropologica Sinica (in Chinese). 37 (1): 146–156. doi:10.16359/j.cnki.cn11-1963/q.2017.0067.
  22. ↑ Shou, Wei-Hua; Qiao, Wn-Fa; Wei, Chuan-Yu; Dong, Yong-Li; Tan, Si-Jie; Shi, Hong; Tang, Wen-Ru; Xiao, Chun-Jie (2010). "Y-chromosome distributions among populations in Northwest China identify significant contribution from Central Asian pastoralists and lesser influence of western Eurasians". J Hum Genet. 55 (5): 314–322. doi: 10.1038/jhg.2010.30 . PMID   20414255. S2CID   23002493.
  23. ↑ Allentoft; et al. (2015). "Population genomics of Bronze Age Eurasia". Nature. 522 (7555): 167–172. Bibcode:2015Natur.522..167A. doi:10.1038/nature14507. PMID   26062507. S2CID   4399103. Archived from the original on 2020-02-04. Retrieved 2020-01-21.
  24. ↑ C. Rоttensteiner, J2a2-PH3085, SK1403: Ancient Altai, modern Uygur and Turkish Archived 2015-06-26 at the Wayback Machine , J2-M172 Haplogroup Research.
  25. ↑ F. Immanuel, Codes for Gedmatch Results, Ancient DNA page Archived 2015-09-05 at the Wayback Machine , F999962 for RISE504, Kytmanovo sample, and F999965 for RISE602, Sary-bel sample.
  26. ↑ Al-Zahery et al, 2011, Additional file 3. Absolute frequencies of Y-chromosome haplogroups and sub-haplogroups in the 48 populations included in the PCA. Archived 2015-11-06 at the Wayback Machine Note: Only 37 of 154 samples (24%) are J2 in Iraq according to the list of Al-Zahery 2011. 43.6% is the frequency of J2 among all J haplogroup Iraqis, not all haplogroups.
  27. ↑ Abu-Amero (2009), Saudi Arabian Y-Chromosome diversity and its relationship with nearby regions Archived 2017-04-03 at the Wayback Machine , Quote: The most abundant haplogroups in Saudi Arabia, J1-M267 (42%), J2-M172 (14%), E1-M2 (8%), R1-M17 (5%) and K2-M184 (5%) are also well represented in other Arabian populations (Table (Table1).1).
  28. 1 2 3 Singh S, Singh A, Rajkumar R, Sampath Kumar K, Kadarkarai Samy S, Nizamuddin S, et al. (January 2016). "Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup". Scientific Reports. 6: 19157. Bibcode:2016NatSR...619157S. doi:10.1038/srep19157. PMC   4709632 . PMID   26754573.
  29. ↑ Herrera, Rene J.; Garcia-Bertrand, Ralph (2018). Ancestral DNA, Human Origins, and Migrations. Academic Press. p. 250. ISBN   978-0-12-804128-4.
  30. 1 2 3 4 Sengupta S, Zhivotovsky LA, King R, Mehdi SQ, Edmonds CA, Chow CE, et al. (February 2006). "Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralists". American Journal of Human Genetics. 78 (2): 202–21. doi:10.1086/499411. PMC   1380230 . PMID   16400607.
  31. ↑ Arunkumar G, Soria-Hernanz DF, Kavitha VJ, Arun VS, Syama A, Ashokan KS, et al. (2012). "Population differentiation of southern Indian male lineages correlates with agricultural expansions predating the caste system". PLOS ONE. 7 (11): e50269. Bibcode:2012PLoSO...750269A. doi: 10.1371/journal.pone.0050269 . PMC   3508930 . PMID   23209694.
  32. ↑ Thanseem I, Thangaraj K, Chaubey G, Singh VK, Bhaskar LV, Reddy BM, et al. (August 2006). "Genetic affinities among the lower castes and tribal groups of India: inference from Y chromosome and mitochondrial DNA". BMC Genetics. 7: 42. doi: 10.1186/1471-2156-7-42 . PMC   1569435 . PMID   16893451.
  33. ↑ Sharma S, Rai E, Sharma P, Jena M, Singh S, Darvishi K, et al. (January 2009). "The Indian origin of paternal haplogroup R1a1* substantiates the autochthonous origin of Brahmins and the caste system". Journal of Human Genetics. 54 (1): 47–55. doi: 10.1038/jhg.2008.2 . PMID   19158816.
  34. 1 2 Qamar R, Ayub Q, Mohyuddin A, et al. (May 2002). "Y-Chromosomal DNA Variation in Pakistan". Am. J. Hum. Genet. 70 (5): 1107–24. doi:10.1086/339929. PMC   447589 . PMID   11898125.
  35. ↑ Shah AM, Tamang R, Moorjani P, Rani DS, Govindaraj P, Kulkarni G, Bhattacharya T, Mustak MS, Bhaskar LV, Reddy AG, Gadhvi D, Gai PB, Chaubey G, Patterson N, Reich D, Tyler-Smith C, Singh L, Thangaraj K (2011). "Indian Siddis: African Descendants with Indian Admixture". Am. J. Hum. Genet. 89 (1): 154–61. doi:10.1016/j.ajhg.2011.05.030. PMC   3135801 . PMID   21741027.
  36. ↑ Toomas Kivisild; Siiri Rootsi; Mait Metspalu; Ene Metspalu; Juri Parik; Katrin Kaldma; Esien Usanga; Sarabjit Mastana; Surinder S. Papiha; Richard Villems (2002). "The Genetics of Language and Farming Spread in India" (PDF). In Peter Bellwood; Colin Renfrew (eds.). Examining the farming/language dispersal hypothesis. McDonald Institute monographs. McDonald Institute for Archaeological Research. ISBN   9781902937205.
  37. ↑ "Ancestry of Maldivian Islanders in Light of Population Genetics: Maldivian Ancestry in light of Genetics". May 24, 2013. Archived from the original on October 29, 2013. Retrieved August 6, 2016.
  38. 1 2 3 Gyaneshwer Chaubey, Manvendra Singh, Federica Crivellaro, et al., "Unravelling the distinct strains of Tharu ancestry." European Journal of Human Genetics (2014), 1–9. doi:10.1038/ejhg.2014.36
  39. ↑ Simona Fornarino, Maria Pala, Vincenza Battaglia, et al., "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation." BMC Evolutionary Biology 2009, 9:154. doi:10.1186/1471-2148-9-154
  40. ↑ Singh, Sakshi; Singh, Ashish; Rajkumar, Raja; Sampath Kumar, Katakam; Kadarkarai Samy, Subburaj; Nizamuddin, Sheikh; Singh, Amita; Ahmed Sheikh, Shahnawaz; Peddada, Vidya; Khanna, Vinee; Veeraiah, Pandichelvam; Pandit, Aridaman; Chaubey, Gyaneshwer; Singh, Lalji; Thangaraj, Kumarasamy (2016-01-12). "Dissecting the influence of Neolithic demic diffusion on Indian Y-chromosome pool through J2-M172 haplogroup". Scientific Reports. 6 (1): 19157. doi: 10.1038/srep19157 . ISSN   2045-2322. PMC   4709632 .
  41. ↑ "Ossetian DNA Project - Y-DNA Classic Chart". familytreedna.
  42. ↑ "Haplogroup J2 (Y-DNA)". The Genetic Atlas. Archived from the original on 2010-09-24. Retrieved 2010-12-27.
  43. ↑ "Y-DNA Haplotree". Archived from the original on 2013-01-27. Retrieved 2013-01-05.Family Tree DNA uses the Y-Chromosome Consortium tree and posts it on their website.

Sources for conversion tables

Notes

  1. ^ Renfrew AC (1998). Archaeology and language: the puzzle of Indo-European origins (Pimlico ed.). London: Pimlico. ISBN   978-0-7126-6612-1.
  2. ^ Nebel A, Filon D, Brinkmann B, Majumder PP, Faerman M, Oppenheim A (2001). "The Y chromosome pool of Jews as part of the genetic landscape of the Middle East". Am. J. Hum. Genet. 69 (5): 1095–112. doi:10.1086/324070. PMC   1274378 . PMID   11573163.
  3. ^ Malaspina P, Tsopanomichalou M, Duman T, Stefan M, Silvestri A, Rinaldi B, et al. (2001). "A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area" (PDF). Ann. Hum. Genet. 65 (Pt 4): 339–49. doi: 10.1046/j.1469-1809.2001.6540339.x . hdl:2108/44448. PMID   11592923. S2CID   221448190.

Bibliography

Phylogenetic notes

  1. ↑ This table shows the historic names for J-M172 in published peer reviewed literature. Note that in Semino 2000 Eu09 is a subclade of Eu10 and in Karafet 2001 24 is a subclade of 23.
    YCC 2002/2008 (Shorthand)J-M172
    Jobling and Tyler-Smith 20009
    Underhill 2000VI
    Hammer 2001Med
    Karafet 200124
    Semino 2000Eu9
    Su 1999H4
    Capelli 2001B
    YCC 2002 (Longhand)J2*
    YCC 2005 (Longhand)J2
    YCC 2008 (Longhand)J2
    YCC 2010r (Longhand)J2
  2. ↑ This table shows the historic names for J-P209 (AKA J-12f2.1 or J-M304) in published peer reviewed literature. Note that in Semino 2000 Eu09 is a subclade of Eu10 and in Karafet 2001 24 is a subclade of 23.
    YCC 2002/2008 (Shorthand)J-P209
    (AKA J-12f2.1 or J-M304)
    Jobling and Tyler-Smith 20009
    Underhill 2000VI
    Hammer 2001Med
    Karafet 200123
    Semino 2000Eu10
    Su 1999H4
    Capelli 2001B
    YCC 2002 (Longhand)J*
    YCC 2005 (Longhand)J
    YCC 2008 (Longhand)J
    YCC 2010r (Longhand)J
  3. ↑ "ISOGG 2018 Y-DNA Haplogroup J". www.isogg.org. Archived from the original on 2017-08-18. Retrieved 2010-04-11.
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