retinal homeobox protein Rx, partial [Homo sapiens]

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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).

Nucleotide
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retinal homeobox protein Rx, partial [Homo sapiens]
retinal homeobox protein Rx, partial [Homo sapiens]
gi|1777226689|gb|QGM77509.1|

Protein
PMC Links for Nucleotide (Select 1677500714) (1)
PMC
Chromosome neighbors for GEO Profiles (Select 92280231) (20)
GEO Profiles
Chromosome neighbors for GEO Profiles (Select 132018122) (20)
GEO Profiles
Nucleotide Links for Protein (Select 297206733) (3)
Nucleotide

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Protein