Entity Details

Primary name KIAA0319
Entity type gene
Source Source Link

Details

PrimaryID9856
RefseqGeneNG_016206
SymbolKIAA0319
NameKIAA0319
Chromosome6
Location6p22.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-11-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsK0319_HUMAN

GO terms

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GOName
GO:0001764 neuron migration
GO:0005769 early endosome
GO:0005886 plasma membrane
GO:0010996 response to auditory stimulus
GO:0016021 integral component of membrane
GO:0030517 negative regulation of axon extension
GO:0030669 clathrin-coated endocytic vesicle membrane
GO:0031410 cytoplasmic vesicle
GO:0031901 early endosome membrane
GO:0033555 multicellular organismal response to stress
GO:0043231 intracellular membrane-bounded organelle
GO:0048692 negative regulation of axon extension involved in regeneration
GO:0060391 positive regulation of SMAD protein signal transduction
GO:0061024 membrane organization
GO:2000171 negative regulation of dendrite development

Diseases

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Disease IDSourceNameDescription
600202 OMIMDyslexia 2 (DYX2)A relatively common, complex cognitive disorder characterized by an impairment of reading performance despite adequate motivational, educational and intellectual opportunities. It is a multifactorial trait, with evidence for familial clustering and heritability. Disease susceptibility is associated with variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
KIAA0319FEM1BBioGRID, HPRD, IntAct12421765 details
KIAA0319SH2B1BioGRID, HPRD, IntAct12421765 details
KIAA0319APPBioGRID, UniProt26960425 details
KIAA0319MYCIntAct21150319 details