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Gene information for NR0B1 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID190
Official gene symbolNR0B1
Full namenuclear receptor subfamily 0, group B, member 1
Aliases,AHC,AHCH,AHX,DAX-1,DAX1,DSS,GTD,HHG,NROB1,
Gene summaryThis gene encodes a protein that contains a DNA-binding domain. The encoded protein acts as a dominant-negative regulator of transcription which is mediated by the retinoic acid receptor. This protein also functions as an anti-testis gene by acting antagonistically to Sry. Mutations in this gene result in both X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism. [provided by RefSeq]
LocationChromosome: X   Locus: Xp21.3-p21.2
Gene position30327495 - 30322539  Map Viewer
Gene orientationminus
Gene size4957 bp
Gene sequence
OMIM ID300473