IFNGR2

protein-coding gene in the species Homo sapiens

Details

Instance of: gene
Subclass of: protein-coding gene
chromosome: human chromosome 21
cytogenetic location: 21q22.11
encodes: Interferon gamma receptor 2
expressed in: monocyte, blood, granulocyte, placenta, tibial nerve, appendix, rectum, gallbladder, spleen, subcutaneous adipose tissue
found in taxon: Homo sapiens
genetic association: obesity, Crohn's disease, mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
genomic end: 33479348, 34851655
genomic start: 34775202, 33403413
HomoloGene ID: 4041
ortholog: Ifngr2, Ifngr2
strand orientation: forward strand

Nothing in the MetaHistoryBook collection references this item yet.