HORMAD2
HORMA domain containing 2 is a protein that in humans is encoded by the HORMAD2 gene.[5]
| HORMAD2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | HORMAD2, CT46.2, HORMA domain containing 2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | MGI: 1923078 HomoloGene: 45130 GeneCards: HORMAD2 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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References
- GRCh38: Ensembl release 89: ENSG00000176635 - Ensembl, May 2017
- GRCm38: Ensembl release 89: ENSMUSG00000020419 - Ensembl, May 2017
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: HORMA domain containing 2". Retrieved 2011-10-22.
Further reading
- Imielinski M, Baldassano RN, Griffiths A, Russell RK, Annese V, Dubinsky M, et al. (December 2009). "Common variants at five new loci associated with early-onset inflammatory bowel disease". Nature Genetics. 41 (12): 1335–40. doi:10.1038/ng.489. PMC 3267927. PMID 19915574.
- Amre DK, Mack DR, Morgan K, Israel D, Deslandres C, Seidman EG, et al. (August 2010). "Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children". Human Genetics. 128 (2): 131–5. doi:10.1007/s00439-010-0835-2. PMID 20473688. S2CID 9303620.
- Gharavi AG, Kiryluk K, Choi M, Li Y, Hou P, Xie J, et al. (March 2011). "Genome-wide association study identifies susceptibility loci for IgA nephropathy" (PDF). Nature Genetics. 43 (4): 321–7. doi:10.1038/ng.787. hdl:11379/67851. PMC 3412515. PMID 21399633.
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