RecName: Full=Zinc finger protein 592

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WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease. [Hum Mutat. 2015]
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney Disease.
Vodopiutz J, Seidl R, Prayer D, Khan MI, Mayr JA, Streubel B, Steiß JO, Hahn A, Csaicsich D, Castro C, et al. Hum Mutat. 2015 Nov; 36(11):1021-8. Epub 2015 Aug 6.
A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze Family. [Neurogenetics. 2002]
A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze Family.
Delague V, Bareil C, Bouvagnet P, Salem N, Chouery E, Loiselet J, Mégarbané A, Claustres M. Neurogenetics. 2002 Mar; 4(1):23-7.
New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family. [Am J Med Genet. 2001]
New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family.
Mégarbané A, Delague V, Ruchoux MM, Rizkallah E, Maurage CA, Viollet L, Rouaix-Emery N, Urtizberea A. Am J Med Genet. 2001 Jun 15; 101(2):135-41.

RefSeq genomic sequence
See the genomic reference sequence for the ZNF592 gene (NG_028094.2).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the ZNF592 gene.

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Q92610 [Domain Mapping of Disease Mut...]
Q92610
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein