Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1406
Gene name Gene Name - the full gene name approved by the HGNC.
Cone-rod homeobox
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CRX
Synonyms (NCBI Gene) Gene synonyms aliases
CORD2, CRD, LCA7, OTX3
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.33
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene 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 thi
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs61748436 G>A Pathogenic, likely-pathogenic Coding sequence variant, missense variant
rs61748449 G>- Not-provided, pathogenic Coding sequence variant, frameshift variant
rs62654391 G>A Not-provided, likely-pathogenic Coding sequence variant, missense variant
rs104894671 A>C Not-provided, pathogenic Coding sequence variant, missense variant
rs104894672 C>T Not-provided, pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT672521 hsa-miR-500a-5p HITS-CLIP 23824327
MIRT672520 hsa-miR-6499-5p HITS-CLIP 23824327
MIRT672519 hsa-miR-24-3p HITS-CLIP 23824327
MIRT672518 hsa-miR-6781-5p HITS-CLIP 23824327
MIRT672517 hsa-miR-3178 HITS-CLIP 23824327
Transcription factors
Transcription factor Regulation Reference
TFAP2A Unknown 12408971
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000785 Component Chromatin ISS
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IEA
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding ISS
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602225 2383 ENSG00000105392
Protein
UniProt ID O43186
Protein name Cone-rod homeobox protein
Protein function Transcription factor that binds and transactivates the sequence 5'-TAATC[CA]-3' which is found upstream of several photoreceptor-specific genes, including the opsin genes. Acts synergistically with other transcription factors, such as NRL, RORB
PDB 9B8U
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00046 Homeodomain 40 96 Homeodomain Domain
PF03529 TF_Otx 139 249 Otx1 transcription factor Family
Tissue specificity TISSUE SPECIFICITY: Retina.
Sequence
MMAYMNPGPHYSVNALALSGPSVDLMHQAVPYPSAPRKQRRERTTFTRSQLEELEALFAK
TQYPDVYAREEVALKINLPESRVQVWFKNRRAKCRQ
QRQQQKQQQQPPGGQAKARPAKRK
AGTSPRPSTDVCPDPLGISDSYSPPLPGPSGSPTTAVATVSIWSPASESPLPEAQRAGLV
ASGPSLTSAPYAMTYAPASAFCSSPSAYGSPSSYFSGLDPYLSPMVPQLGGPALSPLSGP
SVGPSLAQS
PTSLSGQSYGAYSPVDSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL
Sequence length 299
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Cone-rod dystrophy cone-rod dystrophy 2 rs2123743692, rs104894671, rs1568626209, rs104894672, rs749738655, rs281865516, rs61748436, rs1968173024 N/A
Leber Congenital Amaurosis leber congenital amaurosis 7, leber congenital amaurosis, Leber congenital amaurosis 1 rs786205630, rs869312175, rs61748449, rs1599991538, rs1599991611, rs61748446, rs281865515, rs281865517, rs104894673, rs1568626289 N/A
Macular dystrophy macular dystrophy rs1555801963 N/A
retinal dystrophy Retinal dystrophy rs1968165008, rs1968165080, rs2123743692, rs1968169004, rs878853383, rs1968170098, rs62636512, rs1064797247, rs104894672, rs775073228, rs771450991, rs749738655, rs1968169319, rs281865516, rs61748436
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N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Triglyceride levels in non-type 2 diabetes N/A N/A GWAS
Myopathy Central core myopathy N/A N/A ClinVar
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Blindness Associate 11328746, 29568065
Breast Neoplasms Associate 25367122
Cone Rod Dystrophies Associate 10984472, 25082885, 29568065, 30095615, 31203166, 31574917, 32927963, 33910785, 37239417, 9390563, 9427255, 9610810, 9792858
Disease Associate 20513135
Eye Diseases Associate 31626798
Factor V Deficiency Associate 20138881
Genetic Diseases Inborn Associate 34653402
Heart Diseases Associate 34653402
Hemophilia A Associate 20138881
Leber Congenital Amaurosis Associate 10984472, 11328746, 15024725, 18936139, 19753312, 20513135, 21602930, 24066033, 28966547, 29568065, 31247521, 31626798, 32533067, 33513359, 34653402
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