Cone Rod Homeobox Protein (CRX)

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CORD2; CRD; LCA7; OTX3; Orthodenticle Homeobox 3

Cone Rod Homeobox Protein (CRX)
CRX is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.The CRX homeodomain is located near the amino terminus at residues 39 to 99 and belongs to the prd class. Additional domains of the CRX protein include the WSP motif and the OTX tail. The CRX gene was expressed as an abundant 4.5-kb transcript in retina but not in any other of 10 tissues or cells examined.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Cone Rod Homeobox Protein (CRX) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Cone Rod Homeobox Protein (CRX) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Cone Rod Homeobox Protein (CRX) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Cone Rod Homeobox Protein (CRX) CLIA Kit Customized Service Offer
n/a ELISA Kit for Cone Rod Homeobox Protein (CRX) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Cone Rod Homeobox Protein (CRX) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Cone Rod Homeobox Protein (CRX) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Cone Rod Homeobox Protein (CRX) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Cone Rod Homeobox Protein (CRX) CLIA Kit Customized Service Offer
n/a ELISA Kit for Cone Rod Homeobox Protein (CRX) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Cone Rod Homeobox Protein (CRX) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Cone Rod Homeobox Protein (CRX) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Cone Rod Homeobox Protein (CRX) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Cone Rod Homeobox Protein (CRX) CLIA Kit Customized Service Offer
n/a ELISA Kit for Cone Rod Homeobox Protein (CRX) ELISA Kit Customized Service Offer
  1. "Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor."Cell 91:543-553(1997) [PubMed] [Europe PMC] [Abstract]
  2. "The DNA sequence and biology of human chromosome 19." Nature 428:529-535(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "Mapping of transcription start sites of human retina expressed genes."BMC Genomics 8:42-42(2007) [PubMed] [Europe PMC] [Abstract]
  5. "Both PCE-1/RX and OTX/CRX interactions are necessary for photoreceptor-specific gene expression."J. Biol. Chem. 275:1152-1160(2000) [PubMed] [Europe PMC] [Abstract]
  6. "The leucine zipper of NRL interacts with the CRX homeodomain. A possible mechanism of transcriptional synergy in rhodopsin regulation."J. Biol. Chem. 275:29794-29799(2000) [PubMed] [Europe PMC] [Abstract]
  7. "QRX, a novel homeobox gene, modulates photoreceptor gene expression."Hum. Mol. Genet. 13:1025-1040(2004) [PubMed] [Europe PMC] [Abstract]
  8. "Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration."Neuron 19:1329-1336(1997) [PubMed] [Europe PMC] [Abstract]
  9. "A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene."Am. J. Hum. Genet. 63:1307-1315(1998) [PubMed] [Europe PMC] [Abstract]
  10. "Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function."Hum. Mol. Genet. 8:299-305(1999) [PubMed] [Europe PMC] [Abstract]
  11. "The consensus coding sequences of human breast and colorectal cancers." Science 314:268-274(2006) [PubMed] [Europe PMC] [Abstract]
  12. "Molecular characterization of Leber congenital amaurosis in Koreans."Mol. Vis. 14:1429-1436(2008) [PubMed] [Europe PMC] [Abstract]
  13. "Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL."Hum. Mutat. 31:E1472-E1483(2010) [PubMed] [Europe PMC] [Abstract]
  14. "Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis."PLoS ONE 6:E19458-E19458(2011) [PubMed] [Europe PMC] [Abstract]