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Genes search result for Homo sapiens
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1 records found for search term Cirh1a
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1322745UTP4UTP4 small subunit processome componentThis 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 childho166913264969169021Human99old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]