Gene: ENSG00000121351 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000121351
Transcript Identifier
ENST00000240652
Gene Type
Coding gene
Location
12 : 21373352-21378426 : positive

Family Information

Homologous gene family
HOM03P016687
(5 genes in 2 species)
specific family
Duplication type
Block duplicate

Descriptions

gene_descr
islet amyloid polypeptide

Identifiers

Type Value
pidENSP00000240652
HGNC5329
UniprotP10997
UniprotA0A024RAU1

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0019233
IEA
Genome Projectsensory perception of pain
GO:0042755
IEA
Genome Projecteating behavior
GO:0045596
IEA
Genome Projectnegative regulation of cell differentiation
GO:0045779
IEA
Genome Projectnegative regulation of bone resorption
GO:0006915
TAS
Genome Projectapoptotic process
GO:0007165
TAS
Genome Projectsignal transduction
GO:0007267
TAS
Genome Projectcell-cell signaling
GO:0031018
TAS
Genome Projectendocrine pancreas development

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005179
IEA
Genome Projecthormone activity
GO:0005102
TAS
Genome Projectreceptor binding
GO:0042802
IPI
Genome Projectidentical protein binding

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005576
TAS, IEA
Genome Projectextracellular region
GO:0005615
IEA
Genome Projectextracellular space
GO:0043025
IEA
Genome Projectneuronal cell body

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
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InterPro Description
IPR000443Pro-islet amyloid polypeptide
IPR001693Calcitonin peptide-like
IPR018360Calcitonin, conserved site
IPR021116Calcitonin/adrenomedullin
IPR021117Calcitonin-like

No MapMan annotations defined for this gene.