CRB1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[11]
- Cytogenetic location
- 1q31.3[16]
- Expressed in
- ganglionic eminence, ventricular zone, endothelial cell, cerebellar hemisphere, right hemisphere of cerebellum, amygdala, caudate nucleus, anterior cingulate cortex, right frontal lobe, nucleus accumbens[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- retinitis pigmentosa 12, Leber congenital amaurosis 8, pigmented paravenous retinochoroidal atrophy[12][13][14]
- HomoloGene ID
- 8092[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en CRB1
en CRB1-A
en CRB1-B
en CRB1-C
en crumbs 1, cell polarity complex component
en crumbs cell polarity complex component 1
en LCA8
en RP12
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000134376
- Ensembl transcript ID
- ENST00000538660, ENST00000367397, ENST00000367399, ENST00000367400, ENST00000448952, ENST00000475659, ENST00000476483, ENST00000480086, ENST00000484075, ENST00000535699, ENST00000638467, ENST00000681519
- Entrez Gene ID
- 23418
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxflg
- HGNC ID
- 2343
- HGNC gene symbol
- CRB1
- Microsoft Academic ID (discontinued)
- 2780390893
- OMIM ID
- 604210
- RefSeq RNA ID
- XM_011509369, NM_001193640, NM_001257965, NM_001257966, NM_012076, NM_201253, NR_047563, NR_047564, XM_011509365, XM_011509367, XM_017000852, XM_047416572, XM_047416573, XM_047416574, XM_047416575
- UMLS CUI
- C1413701
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