Gene: ENSG00000171444 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000171444
Transcript Identifier
ENST00000408903
Gene Type
Coding gene
Location
5 : 113027302-113488414 : negative

Family Information

Homologous gene family
HOM03P020245
(4 genes in 3 species)
specific family

Descriptions

gene_descr
mutated in colorectal cancers

Identifiers

Type Value
pidENSP00000386227
HGNC6935
UniprotP23508

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0007165
TAS
Genome Projectsignal transduction
GO:0010633
IMP
Genome Projectnegative regulation of epithelial cell migration
GO:0016055
IEA
Genome ProjectWnt signaling pathway
GO:0045184
IDA
Genome Projectestablishment of protein localization
GO:0050680
IDA
Genome Projectnegative regulation of epithelial cell proliferation
GO:0090090
IDA, IMP
Genome Projectnegative regulation of canonical Wnt signaling pathway

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0004872
TAS
Genome Projectreceptor activity
GO:0005515
IPI
Genome Projectprotein binding

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005634
IDA
IEA
Genome Projectnucleus
GO:0005654
IDA
Genome Projectnucleoplasm
GO:0005737
IDA
IEA
Genome Projectcytoplasm
GO:0005886
IDA
IEA
Genome Projectplasma membrane
GO:0016020
IEA
Genome Projectmembrane
GO:0030027
IEA
Genome Projectlamellipodium
GO:0042995
IEA
Genome Projectcell projection

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
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InterPro Description
IPR019536Usher syndrome type-1C protein-binding protein 1, PDZ domain

No MapMan annotations defined for this gene.