Gene: ENSG00000148965 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000148965
Transcript Identifier
ENST00000278222
Gene Type
Coding gene
Location
11 : 18231502-18235926 : negative

Family Information

Homologous gene family
HOM03P009834
(8 genes in 2 species)
specific family
Orthologous gene family
ORTHO03P030650
(3 genes in 2 species)
specific family
Duplication type
Tandem duplicate

Descriptions

gene_descr
serum amyloid A4, constitutive

Identifiers

Type Value
pidENSP00000278222
HGNC10516
UniprotP35542

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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
NAS, 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  
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InterPro Description
IPR000096Serum amyloid A protein

No MapMan annotations defined for this gene.