WRNIP1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | WRNIP1 , WHIP, bA420G6.2, Werner helicase interacting protein 1, WRN helicase interacting protein 1, CFAP93, FAP93 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 608196 MGI: 1926153 HomoloGene: 10592 GeneCards: WRNIP1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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ATPase WRNIP1 is an enzyme that is encoded by the WRNIP1 gene in humans. [5] [6] The protein is a member of AAA ATPase family.
Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging. The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain. This protein shows homology to replication factor C family proteins, and is conserved from E. coli to human. Studies in yeast suggest that this gene may influence the aging process. Two transcript variants encoding different isoforms have been isolated for this gene. [6]
WRNIP1 has been shown to interact with Werner syndrome ATP-dependent helicase. [5]
Ras GTPase-activating protein-binding protein 1 is an enzyme that in humans is encoded by the G3BP1 gene.
NSFL1 cofactor p47 is a protein that in humans is encoded by the NSFL1C gene.
Probable ATP-dependent RNA helicase DDX11 is an enzyme that in humans is encoded by the DDX11 gene.
5'-AMP-activated protein kinase subunit beta-2 is an enzyme that in humans is encoded by the PRKAB2 gene.
Probable ATP-dependent RNA helicase DDX47 is an enzyme that in humans is encoded by the DDX47 gene.
Mitochondrial import receptor subunit TOM34 is a protein that in humans is encoded by the TOMM34 gene.
Putative helicase MOV-10 is an enzyme that in humans is encoded by the MOV10 gene. Stability of MOV10 protein is controlled via DCAF12 ubiquitin ligase.
AP-3 complex subunit sigma-2 is a protein that in humans is encoded by the AP3S2 gene.
Probable ATP-dependent RNA helicase DDX56 is an enzyme that in humans is encoded by the DDX56 gene.
Obg-like ATPase 1 is an enzyme that in humans is encoded by the OLA1 gene. Ola1 belongs to the protein family of Obg-like GTPases but defines an exceptional example of a protein that has evolved altered nucleotide specificity and binds adenosine triphosphate (ATP) with higher affinity than guanosine triphosphate (GTP).
Probable cation-transporting ATPase 13A3 is an enzyme that in humans is encoded by the ATP13A3 gene.
ATP-dependent RNA helicase DDX19B is an enzyme that in humans is encoded by the DDX19B gene.
Kinetochore-associated protein NSL1 homolog is a protein that in humans is encoded by the NSL1 gene.
Zinc finger protein 219 is a protein that in humans is encoded by the ZNF219 gene.
ATP synthase subunit O, mitochondrial is an enzyme that in humans is encoded by the ATP5PO gene.
Centromere protein T is a protein that in humans is encoded by the CENPT gene.
E3 ubiquitin-protein ligase RNF34 is an enzyme that in humans is encoded by the RNF34 gene.
GPI mannosyltransferase 3 is an enzyme that in humans is encoded by the PIGB gene.
Centrosomal protein of 70 kDa is a protein that in humans is encoded by the CEP70 gene. The protein interacts with γ-tubulin through its coiled coil domains to localize at the centrosome. CEP70 is involved in organizing microtubules in interphase cells and is required for proper organization and orientation of the mitotic spindle.
Bardet–Biedl syndrome 10, also known as BBS10 is a human gene.