Gene: ENSG00000164932 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000164932
Transcript Identifier
ENST00000330295
Gene Type
Coding gene
Location
8 : 103371657-103382600 : positive

Family Information

Homologous gene family
HOM03P085089
(orphan gene)
specific family

Descriptions

gene_descr
collagen triple helix repeat containing 1

Identifiers

Type Value
pidENSP00000330523
HGNC18831
UniprotQ96CG8

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0016477
IEA
Genome Projectcell migration
GO:0032092
IEA
Genome Projectpositive regulation of protein binding
GO:0033690
IEA
Genome Projectpositive regulation of osteoblast proliferation
GO:0043932
IEA
Genome Projectossification involved in bone remodeling
GO:0045669
IEA
Genome Projectpositive regulation of osteoblast differentiation
GO:0060071
IEA
Genome ProjectWnt signaling pathway, planar cell polarity pathway
GO:0060122
IEA
Genome Projectinner ear receptor stereocilium organization
GO:0090090
IEA
Genome Projectnegative regulation of canonical Wnt signaling pathway
GO:0090103
IEA
Genome Projectcochlea morphogenesis
GO:0090177
IEA
Genome Projectestablishment of planar polarity involved in neural tube closure

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005109
IEA
Genome Projectfrizzled binding
GO:0017147
IEA
Genome ProjectWnt-protein binding

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005576
IEA
Genome Projectextracellular region
GO:0005578
IEA
Genome Projectproteinaceous extracellular matrix
GO:0005581
IEA
Genome Projectcollagen trimer
GO:0005615
IDA
Genome Projectextracellular space
GO:0005737
IEA
Genome Projectcytoplasm

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
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No InterPro domains detected for this gene.
No MapMan annotations defined for this gene.