HORMAD2

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HORMA domain containing 2
Identifiers
Symbol HORMAD2
External IDs HomoloGene45130 GeneCards: HORMAD2 Gene
Orthologs
Species Human Mouse
Entrez 150280 75828
Ensembl ENSG00000176635 ENSMUSG00000020419
UniProt Q8N7B1 Q5SQP1
RefSeq (mRNA) NM_152510 NM_029458
RefSeq (protein) NP_689723 NP_083734
Location (UCSC) Chr 22:
30.48 – 30.57 Mb
Chr 11:
4.35 – 4.44 Mb
PubMed search [1] [2]

HORMA domain containing 2 is a protein that in humans is encoded by the HORMAD2 gene.[1]

References[edit]

  1. ^ "Entrez Gene: HORMA domain containing 2". Retrieved 2011-10-22. 

Further reading[edit]

  • Imielinski, M.; Baldassano, R. N.; Griffiths, A.; Russell, R. K.; Annese, V.; Dubinsky, M.; Kugathasan, S.; Bradfield, J. P.; Walters, T. D.; Sleiman, P.; Kim, C. E.; Muise, A.; Wang, K.; Glessner, J. T.; Saeed, S.; Zhang, H.; Frackelton, E. C.; Hou, C.; Flory, J. H.; Otieno, G.; Chiavacci, R. M.; Grundmeier, R.; Castro, M.; Latiano, A.; Dallapiccola, B.; Stempak, J.; Abrams, D. J.; Taylor, K.; McGovern, D.; Western Regional Alliance for Pediatric IBD et al. (2009). "Common variants at five new loci associated with early-onset inflammatory bowel disease". Nature Genetics 41 (12): 1335–1340. doi:10.1038/ng.489. PMC 3267927. PMID 19915574.  edit
  • Amre, D. K.; Mack, D. R.; Morgan, K.; Israel, D.; Deslandres, C.; Seidman, E. G.; Lambrette, P.; Costea, I.; Krupoves, A.; Fegury, H.; Dong, J.; Xhu, Z.; Grimard, G.; Levy, E. (2010). "Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children". Human Genetics 128 (2): 131–135. doi:10.1007/s00439-010-0835-2. PMID 20473688.  edit
  • Gharavi, A. G.; Kiryluk, K.; Choi, M.; Li, Y.; Hou, P.; Xie, J.; Sanna-Cherchi, S.; Men, C. J.; Julian, B. A.; Wyatt, R. J.; Novak, J.; He, J. C.; Wang, H.; Lv, J.; Zhu, L.; Wang, W.; Wang, Z.; Yasuno, K.; Gunel, M.; Mane, S.; Umlauf, S.; Tikhonova, I.; Beerman, I.; Savoldi, S.; Magistroni, R.; Ghiggeri, G. M.; Bodria, M.; Lugani, F.; Ravani, P.; Ponticelli, C. (2011). "Genome-wide association study identifies susceptibility loci for IgA nephropathy". Nature Genetics 43 (4): 321–327. doi:10.1038/ng.787. PMC 3412515. PMID 21399633.  edit