Haplogroup E-M75 | |
---|---|
Possible time of origin | 52,300 years BP [1] |
Coalescence age | 37,400 years BP [1] |
Possible place of origin | Africa |
Ancestor | E-M96 |
Descendants | E-M41, E-M54 |
Defining mutations | M75, P68 |
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.
At Prettejohn's Gully, in Nakuru County, Kenya, there were two pastoralists of the early pastoral period; one carried haplogroups E2 (xE2b)/E-M75 and K1a, and another carried haplogroup L3f1b. [2] [3]
At Ilkek Mounds, in Nakuru County, Kenya, a pastoralist of the Pastoral Iron Age carried haplogroups E2 (xE2b)/E-M75 and L0f2a. [2] [3]
At Kisima Farm/C4, in Laikipia County, Kenya, a pastoralist of the Pastoral Iron Age, carried haplogroups E2 (xE2b)/E-M75 and L3h1a1. [2] [3]
At an Anson Street burial site, in Charleston, South Carolina, there were 18 African Americans found who were dated to the 18th century CE. [4] Coosaw, who was of West African and Native American ancestry, carried haplogroups E2b1a-CTS2400 and A2. [4]
Sorted frequency table of E-M75+ populations. Note that a "?" specifies that the sublineage of E-M75 was either untested for or unreported in the relevant study.
Population | Region | Size | E-M75+ | M41+ | M54+ | E-M75+M41-M54- |
---|---|---|---|---|---|---|
Alur [5] | East Africa | 9 | 66.67% | 66.67% | 0.00% | 0.00% |
Hema [5] | East Africa | 18 | 38.89% | 38.89% | 0.00% | 0.00% |
Xhosa [5] | South Africa | 80 | 27.50% | 0.00% | 27.50% | 0.00% |
Rimaibe [6] | Western Africa | 37 | 27.03% | ? | 27.03% | ? |
Mbuti Pygmies [6] | Central Africa | 12 | 25.00% | ? | 25.00% | ? |
Daba [6] | Central Western Africa | 18 | 22.22% | ? | 22.22% | ? |
Eviya [7] | Central Western Africa | 24 | 20.83% | ? | ? | ? |
Zulu [5] | South Africa | 29 | 20.69% | 0.00% | 20.69% | 0.00% |
Bantu (Kenya) [8] | East Africa | 29 | 17.24% | 3.45% | 13.79% | 0.00% |
Ethiopia [9] | East Africa | 88 | 17.05% | 17.05% | 0.00% | 0.00% |
Ganda [5] | East Africa | 26 | 15.38% | 7.69% | 3.85% | 3.85% |
S.Africa [9] | South Africa | 53 | 15.09% | 0.00% | 15.09% | 0.00% |
Comorian Shirazi [10] | East Africa | - | 14.00% | 0.00% | 14.00% | 0.00% |
Akele [7] | Central Western Africa | 50 | 12.00% | ? | ? | ? |
Eshira [7] | Central Western Africa | 42 | 11.90% | ? | ? | ? |
Dama [5] | South Africa | 18 | 11.11% | 0.00% | 5.56% | 5.56% |
Mixed Nilo-Saharan [6] | Central Western Africa | 9 | 11.11% | ? | 11.11% | ? |
Obamba [7] | Central Western Africa | 47 | 10.64% | ? | ? | ? |
Orungu [7] | Central Western Africa | 21 | 9.52% | ? | ? | ? |
Shake [7] | Central Western Africa | 43 | 9.30% | ? | ? | ? |
Senegalese [11] | West Africa | 33 | 9.09% | ? | ? | ? |
Hutu [8] | East Africa | 69 | 8.70% | 4.35% | 4.35% | 0.00% |
Duma [7] | Central Western Africa | 46 | 8.70% | ? | ? | ? |
Malagasy [12] | Madagascar | 35 | 8.57% | 0.00% | 8.57% | 0.00% |
Teke [7] | Central Western Africa | 48 | 8.33% | ? | ? | ? |
C.Africa [9] | Central Africa | 37 | 8.11% | 0.00% | 8.11% | 0.00% |
Mandara [5] | Central Africa | 28 | 7.14% | 0.00% | 7.14% | 0.00% |
Ngoumba [5] | Central Africa | 31 | 6.45% | 0.00% | 6.45% | 0.00% |
!Kung [6] | South Africa | 64 | 6.25% | ? | 6.25% | ? |
Ndumu [7] | Central Western Africa | 36 | 5.56% | ? | ? | ? |
African Americans [11] | North America | 199 | 5.53% | ? | ? | ? |
Fon [8] | West Africa | 100 | 5.00% | 0.00% | 5.00% | 0.00% |
Sudan [9] | East Africa | 40 | 5.00% | 5.00% | 0.00% | 0.00% |
Tsogo [7] | Central Western Africa | 60 | 5.00% | ? | ? | ? |
Ambo [5] | South Africa | 22 | 4.55% | 0.00% | 4.55% | 0.00% |
Mbuti Pygmies [5] | East Africa | 47 | 4.26% | 0.00% | 4.26% | 0.00% |
Tutsi [8] | East Africa | 94 | 4.26% | 0.00% | 4.26% | 0.00% |
Galoa [7] | Central Western Africa | 47 | 4.26% | ? | ? | ? |
Ngumba [7] | Central Western Africa | 24 | 4.17% | ? | ? | ? |
Mossi [6] | Western Africa | 49 | 4.08% | ? | 4.08% | ? |
Khwe [6] | South Africa | 26 | 3.85% | ? | 3.85% | ? |
Sotho-Tswana [5] | South Africa | 28 | 3.57% | 0.00% | 3.57% | 0.00% |
Nzebi [7] | Central Western Africa | 57 | 3.51% | ? | ? | ? |
Punu [7] | Central Western Africa | 58 | 3.45% | ? | ? | ? |
Bakola Pygmies [5] | Central Africa | 33 | 3.03% | 0.00% | 3.03% | 0.00% |
Wolof [5] | West Africa | 34 | 2.94% | 0.00% | 2.94% | 0.00% |
Senegalese [13] | West Africa | 139 | 2.88% | ? | ? | ? |
Mandinka [5] | West Africa | 39 | 2.56% | 0.00% | 0.00% | 2.56% |
Kikuyu & Kamba [5] | East Africa | 42 | 2.38% | 0.00% | 2.38% | 0.00% |
Wairak [8] | East Africa | 43 | 2.33% | 2.33% | 0.00% | 0.00% |
Makina [7] | Central Western Africa | 43 | 2.33% | ? | ? | ? |
Benga [7] | Central Western Africa | 48 | 2.08% | ? | ? | ? |
Shona [5] | South Africa | 49 | 2.04% | 0.00% | 0.00% | 2.04% |
Kota [7] | Central Western Africa | 53 | 1.89% | ? | ? | ? |
Dogon [5] | West Africa | 55 | 1.82% | 0.00% | 1.82% | 0.00% |
Arabs (Oman) [8] | Near East/Asia | 121 | 1.65% | 0.00% | 1.65% | 0.00% |
Ethiopian (Oromo) [13] | East Africa | 78 | 1.28% | ? | ? | ? |
Haplogroup E-M75(xM41,M54) has been found in 6% (1/18) of a sample of Dama from Namibia, [5] 4% (1/26) of a sample of Ganda from Uganda, [5] 3% (1/39) of a sample of Mandinka from Gambia/Senegal, [5] and 2% (1/49) of a sample of Shona from Zimbabwe. [5]
Haplogroup E-M41 has been found mainly in populations of the Great Lakes and Upper Nile regions of Central-East Africa, including 67% (6/9) of a sample of Alur from the DRC, [5] 39% (7/18) of a sample of Hema from the DRC, [5] 17% (15/88) of a sample from Ethiopia, [9] 8% (2/26) of a sample of Ganda from Uganda, [5] 5% (2/40) of a sample from Sudan, [9] 4% (3/69) of a sample of Hutu from Rwanda, [8] 3% (1/29) of a sample of Bantus from Kenya, [8] and 2% (1/43) of a sample of Iraqw from Tanzania. [8] E-M41 has also been identified in noticeable amounts among commercial DNA testers from the Arabian Peninsula and among a few Ashkenazi Jewish males, [14] and also in a male from Lebanon. [15]
Haplogroup E-M54 has been found in 28% (22/80) of a sample of Xhosa from South Africa, [5] 27% (10/37) of a sample of Rimaibe from Burkina Faso, [6] 22% (4/18) of a sample of Daba from northern Cameroon, [6] 21% (6/29) of a sample of Zulu from South Africa, [5] 15% (8/53) of a sample of non-Khoisan Southern Africans, [9] 14% (4/29) of a sample of Bantus from Kenya, [8] 14% of a sample of Comorian Shirazi, [10] 11% (1/9) of a small sample of speakers of Central Sudanic and Saharan languages from northern Cameroon, [6] 9% (3/35) of a sample of Malagasy from Madagascar, [12] 8% (3/37) of a sample from Central Africa, [9] 7% (2/28) of a sample of Mandara from northern Cameroon, [5] 6% (2/31) of a sample of Ngumba from southern Cameroon, [5] 6% (4/64) of a sample of !Kung from South Africa, [6] 6% (1/18) of a sample of Dama from Namibia, [5] 5% (5/100) of a sample of Fon from Benin, [8] 5% (1/22) of a sample of Ambo from Namibia, [5] 4% (3/69) of a sample of Hutu from Rwanda, [8] 4% (4/94) of a sample of Tutsi from Rwanda, [8] 4% (2/47) of a sample of Mbuti from the DRC, [5] 4% (1/26) of a sample of Ganda from Uganda, [5] 4% (1/26) of a sample of Khwe from South Africa, [6] 4% (1/28) of a sample of Sotho-Tswana from South Africa, [5] 3% (1/33) of a sample of Bakola from southern Cameroon, [5] 3% (1/34) of a sample of Wolof from Gambia/Senegal, [5] 3% (2/72) of a sample from Qatar, [16] 2% (1/42) of a sample of Kikuyu and Kamba from Kenya, [5] 2% (1/55) of a sample of Dogon from Mali, [5] and approximately 2% of a sample of 121 Arabs from Oman. [8]
It has been suggested that haplogroup E-M85 Y-chromosomes have spread through Sub-Saharan Africa quite recently based on the fact that Y-STR microsatellite haplotypes associated with these chromosomes show a low degree of differentiation throughout their broad geographic range. Furthermore, the mean variance of STR alleles of E-M85 chromosomes is higher in Central-Western Africans than in the Southern African Khoisan, leading researchers to propose that E-M85 might have been involved in the range expansion of Bantu-speaking peoples from Central-Western Africa toward Southern Africa. [6] [7]
E-M98(xM85) has been found in 4% (2/49) of a sample of Mossi from Burkina Faso. [6]
E-M200 has been found in 25% (3/12) of a small sample of Mbuti from the Democratic Republic of the Congo. [6] According to Figure 4 of Cruciani (2002), all three Bambuti who exhibit the M200 mutation share an identical microsatellite haplotype based on seven STR loci with one another and with some E-M85(xM200) Khoisan (!Kung and/or Khwe) individuals from South Africa. [6]
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 2006 | ISOGG 2007 | ISOGG 2008 | ISOGG 2009 | ISOGG 2010 | ISOGG 2011 | ISOGG 2012 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
E-P29 | 21 | III | 3A | 13 | Eu3 | H2 | B | E* | E | E | E | E | E | E | E | E | E | E |
E-M33 | 21 | III | 3A | 13 | Eu3 | H2 | B | E1* | E1 | E1a | E1a | E1 | E1 | E1a | E1a | E1a | E1a | E1a |
E-M44 | 21 | III | 3A | 13 | Eu3 | H2 | B | E1a | E1a | E1a1 | E1a1 | E1a | E1a | E1a1 | E1a1 | E1a1 | E1a1 | E1a1 |
E-M75 | 21 | III | 3A | 13 | Eu3 | H2 | B | E2a | E2 | E2 | E2 | E2 | E2 | E2 | E2 | E2 | E2 | E2 |
E-M54 | 21 | III | 3A | 13 | Eu3 | H2 | B | E2b | E2b | E2b | E2b1 | - | - | - | - | - | - | - |
E-P2 | 25 | III | 4 | 14 | Eu3 | H2 | B | E3* | E3 | E1b | E1b1 | E3 | E3 | E1b1 | E1b1 | E1b1 | E1b1 | E1b1 |
E-M2 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a* | E3a | E1b1 | E1b1a | E3a | E3a | E1b1a | E1b1a | E1b1a | E1b1a1 | E1b1a1 |
E-M58 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a1 | E3a1 | E1b1a1 | E1b1a1 | E3a1 | E3a1 | E1b1a1 | E1b1a1 | E1b1a1 | E1b1a1a1a | E1b1a1a1a |
E-M116.2 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a2 | E3a2 | E1b1a2 | E1b1a2 | E3a2 | E3a2 | E1b1a2 | E1b1a2 | E1ba12 | removed | removed |
E-M149 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a3 | E3a3 | E1b1a3 | E1b1a3 | E3a3 | E3a3 | E1b1a3 | E1b1a3 | E1b1a3 | E1b1a1a1c | E1b1a1a1c |
E-M154 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a4 | E3a4 | E1b1a4 | E1b1a4 | E3a4 | E3a4 | E1b1a4 | E1b1a4 | E1b1a4 | E1b1a1a1g1c | E1b1a1a1g1c |
E-M155 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a5 | E3a5 | E1b1a5 | E1b1a5 | E3a5 | E3a5 | E1b1a5 | E1b1a5 | E1b1a5 | E1b1a1a1d | E1b1a1a1d |
E-M10 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a6 | E3a6 | E1b1a6 | E1b1a6 | E3a6 | E3a6 | E1b1a6 | E1b1a6 | E1b1a6 | E1b1a1a1e | E1b1a1a1e |
E-M35 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b* | E3b | E1b1b1 | E1b1b1 | E3b1 | E3b1 | E1b1b1 | E1b1b1 | E1b1b1 | removed | removed |
E-M78 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b1* | E3b1 | E1b1b1a | E1b1b1a1 | E3b1a | E3b1a | E1b1b1a | E1b1b1a | E1b1b1a | E1b1b1a1 | E1b1b1a1 |
E-M148 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b1a | E3b1a | E1b1b1a3a | E1b1b1a1c1 | E3b1a3a | E3b1a3a | E1b1b1a3a | E1b1b1a3a | E1b1b1a3a | E1b1b1a1c1 | E1b1b1a1c1 |
E-M81 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b2* | E3b2 | E1b1b1b | E1b1b1b1 | E3b1b | E3b1b | E1b1b1b | E1b1b1b | E1b1b1b | E1b1b1b1 | E1b1b1b1a |
E-M107 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b2a | E3b2a | E1b1b1b1 | E1b1b1b1a | E3b1b1 | E3b1b1 | E1b1b1b1 | E1b1b1b1 | E1b1b1b1 | E1b1b1b1a | E1b1b1b1a1 |
E-M165 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b2b | E3b2b | E1b1b1b2 | E1b1b1b1b1 | E3b1b2 | E3b1b2 | E1b1b1b2a | E1b1b1b2a | E1b1b1b2a | E1b1b1b2a | E1b1b1b1a2a |
E-M123 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b3* | E3b3 | E1b1b1c | E1b1b1c | E3b1c | E3b1c | E1b1b1c | E1b1b1c | E1b1b1c | E1b1b1c | E1b1b1b2a |
E-M34 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b3a* | E3b3a | E1b1b1c1 | E1b1b1c1 | E3b1c1 | E3b1c1 | E1b1b1c1 | E1b1b1c1 | E1b1b1c1 | E1b1b1c1 | E1b1b1b2a1 |
E-M136 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3ba1 | E3b3a1 | E1b1b1c1a | E1b1b1c1a1 | E3b1c1a | E3b1c1a | E1b1b1c1a1 | E1b1b1c1a1 | E1b1b1c1a1 | E1b1b1c1a1 | E1b1b1b2a1a1 |
The following research teams per their publications were represented in the creation of the YCC tree.
This phylogenetic tree of haplogroup subclades is based on the YCC 2008 tree [17] and subsequent published research.
In human genetics, Haplogroup J-M172 or J2 is a Y-chromosome haplogroup which is a subclade (branch) of haplogroup J-M304. 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 in the Caucasus, Anatolia and/or Western Iran.
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.
Haplogroup B (M60) is a human Y-chromosome DNA haplogroup common to paternal lineages in Africa. It is a primary branch of the haplogroup BT.
Haplogroup C is a major Y-chromosome haplogroup, defined by UEPs M130/RPS4Y711, P184, P255, and P260, which are all SNP mutations. It is one of two primary branches of Haplogroup CF alongside Haplogroup F. Haplogroup C is found in ancient populations on every continent except Africa and is the predominant Y-DNA haplogroup among males belonging to many peoples indigenous to East Asia, Central Asia, Siberia, North America and Australia as well as a some populations in Europe, the Levant, and later Japan.
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.
Haplogroup E-V38, also known as E1b1a-V38, is a major human Y-chromosome DNA haplogroup. E-V38 is primarily distributed in Africa. E-V38 has two basal branches, E-M329 and E-M2. E-M329 is a subclade mostly found in East Africa. E-M2 is the predominant subclade in West Africa, Central Africa, Southern Africa, and the region of African Great Lakes; it also occurs at moderate frequencies in North Africa, West Asia, and Southern Europe.
Haplogroup M, AKA M-P256 and Haplogroup K2b1b is a Y-chromosome DNA haplogroup. M-P256 is a descendant haplogroup of Haplogroup K2b1, and is believed to have first appeared between 32,000 to 47,000 years ago.
Haplogroup R, or R-M207, is a Y-chromosome DNA haplogroup. It is both numerous and widespread among modern populations.
In human genetics, Haplogroup O-M268, also known as O1b, is a Y-chromosome DNA haplogroup. Haplogroup O-M268 is a primary subclade of haplogroup O-F265, itself a primary descendant branch of Haplogroup O-M175.
In human genetics, Haplogroup O-M119 is a Y-chromosome DNA haplogroup. Haplogroup O-M119 is a descendant branch of haplogroup O-F265 also known as O1a, one of two extant primary subclades of Haplogroup O-M175. The same clade previously has been labeled as O-MSY2.2.
Haplogroup S-M230, also known as S1a1b, is a Y-chromosome DNA haplogroup. It is by far the most numerically significant subclade of Haplogroup S1a.
Haplogroup E-P147 is a human Y-chromosome DNA haplogroup. Haplogroup E-P147, along with the less common haplogroup E-M75, is one of the two main branches of the older haplogroup E-M96. The E-P147 clade is commonly observed throughout Africa and is divided into two subclades: the less common, haplogroup E-M132, and the more common, haplogroup E-P177.
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-P177 is a human Y-chromosome DNA haplogroup. E-P177 has two known subclades, which are haplogroup E-P2 and haplogroup E-P75.
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 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.
In human population genetics, Y-Chromosome haplogroups define the major lineages of direct paternal (male) lines back to a shared common ancestor in Africa. Men in the same haplogroup share a set of differences, or markers, on their Y-Chromosome, which distinguish them from men in other haplogroups. These UEPs, or markers used to define haplogroups, are SNP mutations. Y-Chromosome Haplogroups all form "family trees" or "phylogenies", with both branches or sub-clades diverging from a common haplogroup ancestor, and also with all haplogroups themselves linked into one family tree which traces back ultimately to the most recent shared male line ancestor of all men alive today, called in popular science Y Chromosome Adam.
In human genetics, Y Haplogroup E-M123 is a Y-chromosome haplogroup, and defined by the single nucleotide polymorphism (SNP) mutation M123. Like its closest relatives within the larger E-M215 haplogroup, E-M123 is found in Asia, Europe and Africa.
Haplogroup A-L1085, also known as haplogroup A0-T is a human Y-DNA haplogroup. It is part of the paternal lineage of almost all humans alive today. The SNP L1085 has played two roles in population genetics: firstly, most Y-DNA haplogroups have diverged from it and; secondly, it defines the undiverged basal clade A-L1085*.
Haplogroup E-M329, also known as E1b1a2, is a human Y-chromosome DNA haplogroup. E-M329 is mostly found in East Africa.
Haplogroup E-M2, also known as E1b1a1-M2, is a human Y-chromosome DNA haplogroup. E-M2 is primarily distributed within Africa followed by West Asia. More specifically, E-M2 is the predominant subclade in West Africa, Central Africa, Southern Africa, and the region of the African Great Lakes; it also occurs at moderate frequencies in North Africa, and the Middle East. E-M2 has several subclades, but many of these subhaplogroups are included in either E-L485 or E-U175. E-M2 is especially common among indigenous Africans who speak Niger-Congo languages, and was spread to Southern Africa and East Africa through the Bantu expansion.