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 Links for Protein (Select 2212255133) (2)
Nucleotide
NF-kappaB inducing kinase [Mus musculus]
NF-kappaB inducing kinase [Mus musculus]
gi|4877963|gb|AAD31512.1|AF143094_1

Protein
HY031737 RIKEN full-length enriched human cDNA library, testis Homo sapiens cDNA...
HY031737 RIKEN full-length enriched human cDNA library, testis Homo sapiens cDNA clone H04D109N20, mRNA sequence
gi|388969498|gnl|dbEST|76854893|dbj 1737.1|

Nucleotide
Taxonomy Links for Protein (Select 206729934) (1)
Taxonomy
Homo sapiens chromosome 1, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 1, GRCh38.p14 Primary Assembly
gi|568815597|gnl|ASM:GCF_000001305| |NC_000001.11||gpp|GPC_000001293.1||gnl|NCBI_GENOMES|1

Nucleotide

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Protein