Entity Details

Primary name CRYGC
Entity type gene
Source Source Link

Details

PrimaryID1420
RefseqGeneNG_008038
SymbolCRYGC
Namecrystallin gamma C
Chromosome2
Location2q33.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1993-01-14
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCRGC_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

Diseases

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Disease IDSourceNameDescription
604307 OMIMCataract 2, multiple types (CTRCT2)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. CTRCT2 includes Coppock-like cataract, among others. Coppock-like cataract is a congenital pulverulent disk-like opacity involving the embryonic nucleus with many tiny white dots in the lamellar portion of the lens. It is usually bilateral and dominantly inherited. In some cases, CTRCT2 is associated with microcornea without any other systemic anomaly or dysmorphism. Microcornea is defined by a corneal diameter inferior to 10 mm in both meridians in an otherwise normal eye. The disease is caused by variants affecting the gene represented in this entry.

Interactions

12 interactions

InteractorPartnerSourcesPublicationsLink
CRYGCCRYABBioGRID, HPRD, MINT, UniProt11700327 12601044 details
CRYGCCRYBB2BioGRID, HPRD, MINT, UniProt11700327 12601044 details
CRYGCCRYAA2MINT, UniProt11700327 12601044 details
CRYGCCRYAABioGRID, HPRD, MINT, UniProt11700327 12601044 15322286 details
CRYGCCRYGCBioGRID, HPRD, UniProt11700327 12601044 details
CRYGCTRIM7BioGRID, IntAct32296183 details
CRYGCCRYGDBioGRID12601044 details
CRYGCHSPB1BioGRID, HPRD11700327 12601044 details
CRYGCHSPB2BioGRID12601044 details
CRYGCMIPBioGRID18004741 details
CRYGCCRYGBBioGRID, IntAct26186194 28514442 details
CRYGCDISC1BioGRID, MINT29961565 details