Gene: ENSG00000101825 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000101825
Transcript Identifier
ENST00000217939
Gene Type
Coding gene
Location
X : 3309716-3343833 : negative

Family Information

Homologous gene family
HOM03P000274
(139 genes in 9 species)
specific family
Orthologous gene family
ORTHO03P034155
(3 genes in 2 species)
specific family

Descriptions

gene_descr
matrix-remodelling associated 5

Identifiers

Type Value
pidENSP00000217939
HGNC7539
UniprotQ9NR99

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0008150
ND
Genome Projectbiological_process

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0003674
ND
Genome Projectmolecular_function

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005576
IEA
Genome Projectextracellular region
GO:0070062
IDA
Genome Projectextracellular exosome

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
Show redundant parents:  
 
InterPro Description
IPR000372Leucine-rich repeat N-terminal domain
IPR000483Cysteine-rich flanking region, C-terminal
IPR001611Leucine-rich repeat
IPR003591Leucine-rich repeat, typical subtype
IPR003598Immunoglobulin subtype 2
IPR003599Immunoglobulin subtype
IPR007110Immunoglobulin-like domain
IPR013098Immunoglobulin I-set
IPR013783Immunoglobulin-like fold

No MapMan annotations defined for this gene.