Entity Details

Primary name ADDG_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9UEY8
EntryNameADDG_HUMAN
FullNameGamma-adducin
TaxID9606
Evidenceevidence at protein level
Length706
SequenceStatuscomplete
DateCreated2000-12-01
DateModified2021-06-02

Ontological Relatives

GenesADD3

GO terms

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GOName
GO:0000794 condensed nuclear chromosome
GO:0005200 structural constituent of cytoskeleton
GO:0005516 calmodulin binding
GO:0005829 cytosol
GO:0005856 cytoskeleton
GO:0005886 plasma membrane
GO:0005903 brush border
GO:0005911 cell-cell junction
GO:0005938 cell cortex
GO:0014069 postsynaptic density
GO:0016020 membrane
GO:0051015 actin filament binding
GO:0051016 barbed-end actin filament capping
GO:0055085 transmembrane transport

Subcellular Location

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Subcellular Location
Cell membrane
Cytoplasm

Domains

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DomainNameCategoryType
IPR001303 Class II aldolase/adducin N-terminalDomainDomain
IPR027772 Gamma-adducinFamilyFamily
IPR036409 Class II aldolase/adducin N-terminal domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
617008 OMIMCerebral palsy, spastic quadriplegic 3 (CPSQ3)A form of cerebral palsy, a group of non-progressive disorders of movement and/or posture resulting from defects in the developing central nervous system. CPSQ3 is an autosomal recessive neurodevelopmental disorder characterized by variable spasticity and cognitive impairment. The disease is caused by variants affecting the gene represented in this entry.