Gene: ENSG00000050555 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000050555
Transcript Identifier
ENST00000361069
Gene Type
Coding gene
Location
9 : 131009215-131091787 : positive

Family Information

Homologous gene family
HOM03P001010
(61 genes in 12 species)
specific family
Orthologous gene family
ORTHO03P018344
(5 genes in 4 species)
specific family
Duplication type
Tandem duplicate

Descriptions

gene_descr
laminin, gamma 3

Identifiers

Type Value
pidENSP00000354360
HGNC6494
UniprotQ9Y6N6

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0000904
IEA
Genome Projectcell morphogenesis involved in differentiation
GO:0007155
IEA
Genome Projectcell adhesion
GO:0007601
IEA
Genome Projectvisual perception
GO:0014002
IEA
Genome Projectastrocyte development
GO:0030198
TAS
Genome Projectextracellular matrix organization
GO:0060041
IEA
Genome Projectretina development in camera-type eye

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005198
TAS
Genome Projectstructural molecule activity

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005576
TAS, IEA
Genome Projectextracellular region
GO:0005578
TAS, IEA
Genome Projectproteinaceous extracellular matrix
GO:0005604
IEA
Genome Projectbasement membrane
GO:0016020
TAS
Genome Projectmembrane

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
Show redundant parents:  
 
InterPro Description
IPR000034Laminin IV
IPR002049Laminin EGF domain
IPR008211Laminin, N-terminal
IPR008979Galactose-binding domain-like

No MapMan annotations defined for this gene.