Entity Details

Primary name CRYGS
Entity type gene
Source Source Link

Details

PrimaryID1427
RefseqGeneNG_009829
SymbolCRYGS
Namecrystallin gamma S
Chromosome3
Location3q27.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1993-01-19
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCRYGS_HUMAN

GO terms

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GOName
GO:0002009 morphogenesis of an epithelium
GO:0002088 lens development in camera-type eye
GO:0005212 structural constituent of eye lens
GO:0007601 visual perception

Diseases

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Disease IDSourceNameDescription
116100 OMIMCataract 20, multiple types (CTRCT20)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. CTRCT20 includes progressive polymorphic anterior, posterior, or peripheral cortical. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
CRYGSTERF2IPbhf-ucl, BioGRID21044950 details
CRYGSTINF2bhf-ucl, BioGRID21044950 details
CRYGSPOT1bhf-ucl, BioGRID21044950 details
CRYGSCRYABBioGRID, DIP24183572 details