Entity Details

Primary name CRBA1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP05813
EntryNameCRBA1_HUMAN
FullNameBeta-crystallin A3
TaxID9606
Evidenceevidence at protein level
Length215
SequenceStatuscomplete
DateCreated1988-11-01
DateModified2021-06-02

Ontological Relatives

GenesCRYBA1

GO terms

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GOName
GO:0001818 negative regulation of cytokine production
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:0014067 negative regulation of phosphatidylinositol 3-kinase signaling
GO:0032007 negative regulation of TOR signaling
GO:0051898 negative regulation of protein kinase B signaling
GO:0070373 negative regulation of ERK1 and ERK2 cascade
GO:2000210 positive regulation of anoikis

Subcellular Location

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Domains

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DomainNameCategoryType
IPR001064 Beta/gamma crystallinDomainDomain
IPR011024 Gamma-crystallin-likeFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
600881 OMIMCataract 10, multiple types (CTRCT10)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. CTRCT10 includes congenital zonular with sutural opacities, among others. This is a form of zonular cataract with an erect Y-shaped anterior and an inverted Y-shaped posterior sutural opacities. Zonular or lamellar cataracts are opacities, broad or narrow, usually consisting of powdery white dots affecting only certain layers or zones between the cortex and nucleus of an otherwise clear lens. The opacity may be so dense as to render the entire central region of the lens completely opaque, or so translucent that vision is hardly if at all impeded. Zonular cataracts generally do not involve the embryonic nucleus, though sometimes they involve the fetal nucleus. Usually sharply separated from a clear cortex outside them, they may have projections from their outer edges known as riders or spokes. The disease is caused by variants affecting the gene represented in this entry.

Interactions

26 interactions

InteractorPartnerSourcesPublicationsLink
CRBA1_HUMANCRYAB_HUMANBioGRID, MINT17046756 19401464 details
CRBA1_HUMANCRBA1_HUMANBioGRID, HPRD, MINT17662718 19401464 8961355 details
CRBA1_HUMANCRBB1_HUMANBioGRID, HPRD, IntAct, MINT17662718 21516116 25416956 25910212 details
CRBA1_HUMANCRBB2_HUMANBioGRID, HPRD, IntAct, MINT17662718 32296183 details
CRBA1_HUMANCRBB3_HUMANBioGRID, HPRD, IntAct, MINT17662718 25416956 32296183 details
CRBA1_HUMANRBPMS_HUMANBioGRID, IntAct25416956 details
CRBA1_HUMANRHXF2_HUMANBioGRID, IntAct25416956 details
CRBA1_HUMANCRTP1_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANBAFL_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANVAC14_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANFOXH1_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANARI5A_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANPKHF2_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANHXC8_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANKR133_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANKR132_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANCHCH2_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANKR111_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANPROP1_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANCERK1_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANNOXA1_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANCELF6_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANLASP1_HUMANBioGRID, IntAct32296183 details
CRBA1_HUMANCRYA2_HUMANBioGRID19401464 26657544 details
CRBA1_HUMANCRYAA_HUMANBioGRID19401464 26657544 details
CRBA1_HUMANYPEL3_HUMANBioGRID32296183 details