APOL2

Last updated
APOL2
Identifiers
Aliases APOL2 , APOL-II, APOL3, apolipoprotein L2
External IDs OMIM: 607252 MGI: 2444921 HomoloGene: 12785 GeneCards: APOL2
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_030882
NM_145637

NM_001081970
NM_001357895
NM_001357896

RefSeq (protein)

NP_112092
NP_663612

n/a

Location (UCSC) Chr 22: 36.23 – 36.24 Mb Chr 15: 77.63 – 77.64 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Apolipoprotein L2 is a protein that in humans is encoded by the APOL2 gene. [5] [6] [7]

Contents

This gene is a member of the apolipoprotein L gene family and protein in this family are lipid-binding proteins. This gene encodes a 37.1 kDa protein and The protein sequence contains 337bp. Localization of this protein is mainly found in the cytosol, nucleoplasm and additionally, it is also seen in the Nuclear bodies. [8] The involvement of this gene may affect in the movement of lipids and binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene. [7]

Amino Acid Sequence

[9] [10] MNPESSIFIE DYLKYFQDQV SRENLLQLLT DDEAWNGFVA AAELPRDEAD ELRKALNKLA SHMVMKDKNR HDKDQQHRQW FLKEFPRLKR ELEDHIRKLR ALAEEVEQVH RGTTIANVVS NSVGTTSGIL TLLGLGLAPF TEGISFVLLD TGMGLGAAAA VAGITCSVVE LVNKLRARAQ ARNLDQSGTN VAKVMKEFVG GNTPNVLTLV DNWYQVTQGI GRNIRAIRRA RANPQLGAYA PPPHVIGRIS AEGGEQVERV VEGPAQAMSR GTMIVGAATG GILLLLDVVS LAYESKHLLE GAKSESAEEL KKRAQELEGK LNFLTKIHEM LQPGQDQ

Total amino acids: 337 [9]

Interactions

APOL2 has been shown to interact with:

Splice Variants

ApoL2 has 5 splice variants, [15]

This transcript has got 6 exons, 12 domains and features are annotated, 263 variations are related this and maps to 35 oligo probes.

This transcript has got 5 exons, 12 domains and features are annotated, 263 variations are related with this gene and maps to 37 oligo probes.

This transcript has got 6 exons, is annotated with 3 domains and features, 62 variations are related with this gene and maps to 20 oligo probes.

This transcript has got 6 exons, 12 domains and features are annotated, 331 variations are related with this gene and maps to 32 oligo probes.

This transcript has got 5 exons, 4 domains and features are annotated, 104 variations are related with this gene and maps to 13 oligo probes.

Functions of the ApoL2

Related Research Articles

<span class="mw-page-title-main">Apolipoprotein B</span> Protein-coding gene in the species Homo sapiens

Apolipoprotein B (ApoB) is a protein that in humans is encoded by the APOB gene. It is commonly used to detect risk of atherosclerotic cardiovascular disease.

<span class="mw-page-title-main">Apolipoprotein C-III</span> Protein-coding gene in the species Homo sapiens

Apolipoprotein C-III also known as apo-CIII, and apolipoprotein C3, is a protein that in humans is encoded by the APOC3 gene. Apo-CIII is secreted by the liver as well as the small intestine, and is found on triglyceride-rich lipoproteins such as chylomicrons, very low density lipoprotein (VLDL), and remnant cholesterol.

<span class="mw-page-title-main">Apolipoprotein C-IV</span> Protein-coding gene in the species Homo sapiens

Apolipoprotein C-IV, also known as apolipoprotein C4, is a protein that in humans is encoded by the APOC4 gene.

<span class="mw-page-title-main">Apolipoprotein A-II</span> Protein-coding gene in the species Homo sapiens

Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene. It is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. ApoA-II regulates many steps in HDL metabolism, and its role in coronary heart disease is unclear. Remarkably, defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia.

<span class="mw-page-title-main">Phospholipid transfer protein</span> Mammalian protein found in Homo sapiens

Phospholipid transfer protein is a protein that in humans is encoded by the PLTP gene.

<span class="mw-page-title-main">USF1</span> Protein-coding gene in the species Homo sapiens

Upstream stimulatory factor 1 is a protein that in humans is encoded by the USF1 gene.

<span class="mw-page-title-main">CUTL1</span> Protein-coding gene in the species Homo sapiens

Cux1 is a homeodomain protein that in humans is encoded by the CUX1 gene.

<span class="mw-page-title-main">Annexin A7</span> Protein-coding gene in the species Homo sapiens

Annexin A7 is a protein that in humans is encoded by the ANXA7 gene.

<span class="mw-page-title-main">OSBPL3</span> Protein-coding gene in the species Homo sapiens

Oxysterol-binding protein-related protein 3 is a protein that in humans is encoded by the OSBPL3 gene.

<span class="mw-page-title-main">CDK5RAP2</span> Protein with roles in formation and stability of microtubules

CDK5 regulatory subunit-associated protein 2 is a protein that in humans is encoded by the CDK5RAP2 gene. It has necessary roles in the formation and stability of microtubules from the centrosome and has been found to be linked to human brain size variation in males. Multiple transcript variants exist for this gene, but the full-length nature of only two has been determined.

<span class="mw-page-title-main">60S ribosomal protein L8</span> Protein found in humans

60S ribosomal protein L8 is a protein that in humans is encoded by the RPL8 gene.

<span class="mw-page-title-main">SLC35C2</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 35 member C2 is a protein that in humans is encoded by the SLC35C2 gene.

<span class="mw-page-title-main">PTGFRN</span> Protein-coding gene in the species Homo sapiens

Prostaglandin F2 receptor negative regulator is a protein that in humans is encoded by the PTGFRN gene. PTGFRN has also been designated as CD315.

<span class="mw-page-title-main">APOL6</span> Protein-coding gene in the species Homo sapiens

Apolipoprotein L6 is a protein that in humans is encoded by the APOL6 gene.

<span class="mw-page-title-main">PCDHB7</span> Protein-coding gene in the species Homo sapiens

Protocadherin beta-7 is a protein that in humans is encoded by the PCDHB7 gene.

<span class="mw-page-title-main">ZNF41</span> Protein-coding gene in the species Homo sapiens

Zinc finger protein 41 is a protein that in humans is encoded by the ZNF41 gene.

<span class="mw-page-title-main">APOL3</span> Protein-coding gene in the species Homo sapiens

Apolipoprotein L3 is a protein that in humans is encoded by the APOL3 gene. Expressed in the gut, it has antibiotic properties.

<span class="mw-page-title-main">APOF</span> Protein-coding gene in the species Homo sapiens

Apolipoprotein F is a protein that in humans is encoded for by the APOF gene. The product of this gene is one of the minor apolipoproteins found in plasma. This protein forms complexes with lipoproteins and may be involved in transport and/or esterification of cholesterol.

<span class="mw-page-title-main">CEP97</span> Protein-coding gene in the species Homo sapiens

Centrosomal protein of 97 kDa (Cep97), also known as leucine-rich repeat and IQ domain-containing protein 2 (LRRIQ2), is a protein that in humans is encoded by the CEP97 gene.

<span class="mw-page-title-main">GPX5</span> Protein-coding gene in the species Homo sapiens

Glutathione peroxidase 5 (GPx-5), also known as epididymal secretory glutathione peroxidase is an enzyme that in humans is encoded by the GPX5 gene.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000128335 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000056656 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Dunham I, Shimizu N, Roe BA, Chissoe S, Hunt AR, Collins JE, Bruskiewich R, Beare DM, Clamp M, Smink LJ, Ainscough R, Almeida JP, Babbage A, Bagguley C, Bailey J, Barlow K, Bates KN, Beasley O, Bird CP, Blakey S, Bridgeman AM, Buck D, Burgess J, Burrill WD, O'Brien KP, et al. (Dec 1999). "The DNA sequence of human chromosome 22". Nature. 402 (6761): 489–95. Bibcode:1999Natur.402..489D. doi: 10.1038/990031 . PMID   10591208.
  6. Page NM, Butlin DJ, Lomthaisong K, Lowry PJ (May 2001). "The human apolipoprotein L gene cluster: identification, classification, and sites of distribution". Genomics. 74 (1): 71–8. doi:10.1006/geno.2001.6534. PMID   11374903.
  7. 1 2 "Entrez Gene: APOL2 apolipoprotein L, 2".
  8. "The Human Protein atlas Gene: APOL2 apolipoprotein L, 2".
  9. 1 2 "UniProt". www.uniprot.org. Retrieved 2024-02-06.
  10. Ultsch, Mark; Holliday, Michael J.; Gerhardy, Stefan; Moran, Paul; Scales, Suzie J.; Gupta, Nidhi; Oltrabella, Francesca; Chiu, Cecilia; Fairbrother, Wayne; Eigenbrot, Charles; Kirchhofer, Daniel (2021-07-27). "Structures of the ApoL1 and ApoL2 N-terminal domains reveal a non-classical four-helix bundle motif". Communications Biology. 4 (1): 1–16. doi:10.1038/s42003-021-02387-5. ISSN   2399-3642.
  11. Liao W, Goh FY, Betts RJ, Kemeny DM, Tam J, Bay BH, Wong WS (February 2011). "A novel anti-apoptotic role for apolipoprotein L2 in IFN-gamma-induced cytotoxicity in human bronchial epithelial cells". J Cell Physiol. 226 (2): 397–406. doi:10.1002/jcp.22345. PMID   20665705. S2CID   27845807.
  12. Bruening J, Lasswitz L, Banse P, Kahl S, Marinach C, Vondran FW, Kaderali L, Silvie O, Pietschmann T, Meissner F, Gerold G (July 2018). "Hepatitis C virus enters liver cells using the CD81 receptor complex proteins calpain-5 and CBLB". PLOS Pathogens. 14 (7): 55–67. doi: 10.1371/journal.ppat.1007111 . PMC   6053247 . PMID   30024968.
  13. Smith EE, Malik HS (May 2009). "The apolipoprotein L family of programmed cell death and immunity genes rapidly evolved in primates at discrete sites of host-pathogen interactions". Genome Res. 19 (5): 850–8. doi:10.1101/gr.085647.108. PMC   2675973 . PMID   19299565.
  14. 1 2 Liu Z, Lu H, Jiang Z, Pastuszyn A, Hu CA (January 2005). "Apolipoprotein l6, a novel proapoptotic Bcl-2 homology 3-only protein, induces mitochondria-mediated apoptosis in cancer cells". Mol Cancer Res. 3 (1): 21–31. doi: 10.1158/1541-7786.21.3.1 . PMID   15671246. S2CID   2545675.
  15. "The Human Protein atlas Gene: APOL2 apolipoprotein L, 2".
  16. Rao SK, Pavicevic Z, Du Z, Kim JG, Fan M, Jiao Y, Rosebush M, Samant S, Gu W, Pfeffer LM, Nosrat CA (October 2010). "Pro-inflammatory genes as biomarkers and therapeutic targets in oral squamous cell carcinoma". J Biol Chem. 285 (42): 32512–21. doi: 10.1074/jbc.M110.150490 . PMC   2952253 . PMID   20702412.
  17. Liu Z, Lu H, Jiang Z, Pastuszyn A, Hu CA (October 2013). "Mitochondrial proteomic analysis of human host cells infected with H3N2 swine influenza virus". J Proteomics. 8 (91): 136–50. doi:10.1016/j.jprot.2013.06.037. PMID   23856606.
  18. Wang K, Edmondson AC, Li M, Gao F, Qasim AN, Devaney JM, Burnett MS, Waterworth DM, Mooser V, Grant SF, Epstein SE, Reilly MP, Hakonarson H, Rader DJ (July 2011). "Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation". Frontiers in Genetics. 2 (4): 41. doi: 10.3389/fgene.2011.00041 . PMC   3268595 . PMID   22303337.
  19. Brosens JJ, Hodgetts A, Feroze-Zaidi F, Sherwin JR, Fusi L, Salker MS, Higham J, Rose GL, Kajihara T, Young SL, Lessey BA, Henriet P, Langford PR, Fazleabas AT (April 2010). "Proteomic analysis of endometrium from fertile and infertile patients suggests a role for apolipoprotein A-I in embryo implantation failure and endometriosis". MHR: Basic Science of Reproductive Medicine. 16 (4): 273–285. doi:10.1093/molehr/gap108. PMC   2834406 . PMID   20008415.
  20. 1 2 "Nextprot Gene: APOL2 apolipoprotein L, 2".
  21. Luo, Audrey; Jung, Jeesun; Longley, Martha; Rosoff, Daniel B.; Charlet, Katrin; Muench, Christine; Lee, Jisoo; Hodgkinson, Colin A.; Goldman, David; Horvath, Steve; Kaminsky, Zachary A.; Lohoff, Falk W. (2020). "Epigenetic aging is accelerated in alcohol use disorder and regulated by genetic variation in APOL2". Neuropsychopharmacology. 45 (2): 327–336. doi:10.1038/s41386-019-0500-y. PMC   6901591 . PMID   31466081.

Further reading