HORMAD2

HORMAD2
Identifiers
Aliases	HORMAD2 , CT46.2, HORMA domain containing 2
External IDs	MGI: 1923078; HomoloGene: 45130; GeneCards: HORMAD2; OMA:HORMAD2 - orthologs
Gene location (Human) Chr. Chromosome 22 (human) [1] Band 22q12.2 Start 30,080,464 bp [1] End 30,177,075 bp [1]
Gene location (Mouse) Chr. Chromosome 11 (mouse) [2] Band 11|11 A1 Start 4,295,814 bp [2] End 4,391,105 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right testis left testis sperm testicle retinal pigment epithelium mucosa of ileum tibialis anterior muscle right lobe of liver caudate nucleus ventricular zone Top expressed in spermatocyte spermatid embryo embryo zygote yolk sac morula secondary oocyte seminiferous tubule epiblast More reference expression data BioGPS n/a
Orthologs Species Human Mouse Entrez 150280 75828 Ensembl ENSG00000176635 ENSMUSG00000020419 UniProt Q8N7B1 Q5SQP1 RefSeq (mRNA) NM_152510 NM_001329457 NM_001329458 NM_029458 RefSeq (protein) NP_001316386 NP_001316387 NP_689723 NP_083734 Location (UCSC) Chr 22: 30.08 – 30.18 Mb Chr 11: 4.3 – 4.39 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

HORMA domain containing 2 is a protein that in humans is encoded by the HORMAD2 gene. ^[5]

References

1. GRCh38: Ensembl release 89: ENSG00000176635 – Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000020419 – 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. "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.