RecName: Full=Retinal homeobox protein Rx; AltName: Full=Retina and an - Protein

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Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations. [Sci Rep. 2017]
Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations.
Huang XF, Huang ZQ, Lin D, Dai ML, Wang QF, Chen ZJ, Jin ZB, Wang Y. Sci Rep. 2017 Aug 22; 7(1):9064. Epub 2017 Aug 22.
RAX and anophthalmia in humans: evidence of brain anomalies. [Mol Vis. 2012]
RAX and anophthalmia in humans: evidence of brain anomalies.
Abouzeid H, Youssef MA, Bayoumi N, ElShakankiri N, Marzouk I, Hauser P, Schorderet DF. Mol Vis. 2012; 18:1449-56. Epub 2012 Jun 2.
Mutations in the newly identified RAX regulatory sequence are not a frequent cause of micro/anophthalmia. [Genet Test Mol Biomarkers. 2009]
Mutations in the newly identified RAX regulatory sequence are not a frequent cause of micro/anophthalmia.
Chassaing N, Vigouroux A, Calvas P. Genet Test Mol Biomarkers. 2009 Jun; 13(3):289-90.

RefSeq genomic sequence
See the genomic reference sequence for the RAX gene (NG_013031.1).
RefSeq protein
See the reference protein sequence for retinal homeobox protein Rx (NP_038463.2).

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Q9Y2V3 [Domain Mapping of Disease Mut...]
Q9Y2V3
Domain Mapping of Disease Mutations
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reagents [ExactAntigen/Labome]
reagents
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Protein