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Gene information for CIRH1A (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID84916
Official gene symbolCIRH1A
Full namecirrhosis, autosomal recessive 1A (cirhin)
Aliases,CIRHIN,FLJ14728,FLJ17146,KIAA1988,NAIC,TEX292,
Gene summaryThis gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. [provided by RefSeq]
LocationChromosome: 16   Locus: 16q22.1
Gene position69166499 - 69202937  Map Viewer
Gene orientationplus
Gene size36439 bp
Gene sequence
OMIM ID607456