Gene: ENSG00000134339 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000134339
Transcript Identifier
ENST00000526900
Gene Type
Coding gene
Location
11 : 18245377-18248011 : negative

Family Information

Homologous gene family
HOM03P009834
(8 genes in 2 species)
specific family
Orthologous gene family
ORTHO03P024578
(4 genes in 2 species)
specific family
Duplication type
Tandem duplicate

Descriptions

gene_descr
serum amyloid A2

Identifiers

Type Value
pidENSP00000436126
HGNC10514
UniprotP0DJI9

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0006953
IEA
Genome Projectacute-phase response
GO:0050918
IBA
Genome Projectpositive chemotaxis
GO:0060326
IBA
Genome Projectcell chemotaxis

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0042056
IBA
Genome Projectchemoattractant activity

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005576
IEA
Genome Projectextracellular region
GO:0005615
IBA
Genome Projectextracellular space
GO:0034364
IEA
Genome Projecthigh-density lipoprotein particle
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
IPR000096Serum amyloid A protein

No MapMan annotations defined for this gene.