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CRB1

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Crumbs homolog 1 is a protein that in humans is encoded by the CRB1 gene.[5][6][7]

AliasesCRB1, LCA8, RP12, crumbs 1, cell polarity complex component, crumbs cell polarity complex component 1, CRB1-B, CRB1-C, CRB1-A
External IDsOMIM: 604210; MGI: 2136343; GeneCards: CRB1
PDBOrtholog search: PDBe RCSB
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CRB1
Identifiers
AliasesCRB1, LCA8, RP12, crumbs 1, cell polarity complex component, crumbs cell polarity complex component 1, CRB1-B, CRB1-C, CRB1-A
External IDsOMIM: 604210; MGI: 2136343; GeneCards: CRB1
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001193640
NM_001257965
NM_001257966
NM_012076
NM_201253

NM_133239

RefSeq (protein)

NP_001180569
NP_001244894
NP_001244895
NP_957705

NP_573502

Location (UCSC)Chr 1: 197.27 – 197.48 MbChr 1: 139.2 – 139.38 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a protein which is similar to the Drosophila crumbs protein and localizes to the inner segment of mammalian photoreceptors. In Drosophila, crumbs localizes to the stalk of the fly photoreceptor and may be a component of the molecular scaffold that controls proper development of polarity in the eye. Mutations in this gene are associated with a severe form of retinitis pigmentosa, RP12, and with Leber congenital amaurosis. Alternatively spliced transcript variants have been observed but their full-length nature has yet to be determined.[7] One small study suggests that mutations in this gene are associated with keratoconus in patients that already have Leber's congenital amaurosis.[8]

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