RecName: Full=Glutaredoxin domain-containing cysteine-rich protein 1

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Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness. [Ann Otol Rhinol Laryngol. 2015]
Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizziness.
Mori K, Miyanohara I, Moteki H, Nishio SY, Kurono Y, Usami S. Ann Otol Rhinol Laryngol. 2015 May; 124 Suppl 1:129S-34S. Epub 2015 Mar 23.
Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. [Am J Hum Genet. 2010]
Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.
Schraders M, Lee K, Oostrik J, Huygen PL, Ali G, Hoefsloot LH, Veltman JA, Cremers FP, Basit S, Ansar M, et al. Am J Hum Genet. 2010 Feb 12; 86(2):138-47. Epub 2010 Feb 4.
Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus. [Audiol Neurootol. 2004]
Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus.
Odeh H, Hagiwara N, Skynner M, Mitchem KL, Beyer LA, Allen ND, Brilliant MH, Lebart MC, Dolan DF, Raphael Y, et al. Audiol Neurootol. 2004 Sep-Oct; 9(5):303-14. Epub 2004 Sep 3.

RefSeq genomic sequence
See the genomic reference sequence for the GRXCR1 gene (NG_027718.1).
RefSeq protein
See the reference protein sequence for glutaredoxin domain-containing cysteine-rich protein 1 (NP_001073945.1).

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A8MXD5 [Domain Mapping of Disease Mut...]
A8MXD5
Domain Mapping of Disease Mutations
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RecName: Full=Glutaredoxin domain-containing cysteine-rich protein 1
RecName: Full=Glutaredoxin domain-containing cysteine-rich protein 1
gi|205780623|sp|A8MXD5.1|GRCR1_HUMA

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