PREDICTED: Rattus norvegicus glutaredoxin and cysteine rich domain con - Nucleotide

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GRXCR2 Regulates Taperin Localization Critical for Stereocilia Morphology and Hearing. [Cell Rep. 2018]
GRXCR2 Regulates Taperin Localization Critical for Stereocilia Morphology and Hearing.
Liu C, Luo N, Tung CY, Perrin BJ, Zhao B. Cell Rep. 2018 Oct 30; 25(5):1268-1280.e4.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. [Brief Bioinform. 2011]
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD. Brief Bioinform. 2011 Sep; 12(5):449-62. Epub 2011 Aug 27.
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. [Am J Hum Genet. 2010]
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse.
Odeh H, Hunker KL, Belyantseva IA, Azaiez H, Avenarius MR, Zheng L, Peters LM, Gagnon LH, Hagiwara N, Skynner MJ, et al. Am J Hum Genet. 2010 Feb 12; 86(2):148-60. Epub 2010 Feb 4.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the Grxcr1 gene (NM_001191935.1).
RefSeq protein product
See the reference protein sequence for glutaredoxin domain-containing cysteine-rich protein 1 isoform X1 (XP_038948214.1).

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Protein sequence from Nucleotide coding region
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PREDICTED: Rattus norvegicus glutaredoxin and cysteine rich domain containing 1 ...
PREDICTED: Rattus norvegicus glutaredoxin and cysteine rich domain containing 1 (Grxcr1), transcript variant X1, mRNA
gi|1958676880|ref|XM_039092286.1|

Nucleotide
UI-R-CN1-cjh-a-04-0-UI.s1 UI-R-CN1 Rattus norvegicus cDNA clone UI-R-CN1-cjh-a-0...
UI-R-CN1-cjh-a-04-0-UI.s1 UI-R-CN1 Rattus norvegicus cDNA clone UI-R-CN1-cjh-a-04-0-UI 3', mRNA sequence
gi|18186834|gnl|dbEST|10814274|gb|B 81.1|

Nucleotide
Autosomal dominant Kenny-Caffey syndrome
Autosomal dominant Kenny-Caffey syndrome

MedGen
Martsolf syndrome 2
Martsolf syndrome 2

MedGen
Autosomal dominant vitreoretinochoroidopathy
Autosomal dominant vitreoretinochoroidopathy

MedGen

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Nucleotide