Entity Details

Primary name CRYGB
Entity type gene
Source Source Link

Details

PrimaryID1419
RefseqGeneNG_028158
SymbolCRYGB
Namecrystallin gamma B
Chromosome2
Location2q33.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1993-01-14
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCRGB_HUMAN

GO terms

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GOName
GO:0002088 lens development in camera-type eye
GO:0005212 structural constituent of eye lens
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0007601 visual perception
GO:0070309 lens fiber cell morphogenesis

Diseases

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Disease IDSourceNameDescription
615188 OMIMCataract 39, multiple types (CTRCT39)An opacification of the crystalline lens of the eye that frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. CTRCT39 includes lamellar, anterior polar, and complete cataracts. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
CRYGBCRYGCBioGRID, IntAct26186194 28514442 details