CIRH1A 抗体
(Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
This 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, Jul 2008].
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Latest Publications for our CIRH1A 抗体
: "NOL11, implicated in the pathogenesis of North American Indian childhood cirrhosis, is required for pre-rRNA transcription and processing." in: PLoS genetics, Vol. 8, Issue 8, pp. e1002892, (2012) (PubMed).Aliases for CIRH1A 抗体
UTP4, small subunit processome component (UTP4) 抗体UTP4 small subunit processome component (Utp4) 抗体
UTP4 small subunit processome component (utp4) 抗体
UTP4, small subunit processome component (utp4) 抗体
UTP4 small subunit processome component L homeolog (utp4.L) 抗体
CIRH1A 抗体
cirhin 抗体
Cirhin 抗体
CIRHIN 抗体
Naic 抗体
naic 抗体
NAIC 抗体
Teg-292 抗体
Tex292 抗体
tex292 抗体
TEX292 抗体
UTP4 抗体
wu:fi09g10 抗体
wu:fi37c02 抗体
zgc:77199 抗体
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