Gene: ENSG00000196998 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000196998
Transcript Identifier
ENST00000322995
Gene Type
Coding gene
Location
X : 49074803-49078095 : negative

Family Information

Homologous gene family
HOM03P000706
(78 genes in 36 species)
specific family
Orthologous gene family
ORTHO03P064683
(2 genes in 2 species)
specific family

Descriptions

gene_descr
WD repeat domain 45

Identifiers

Type Value
pidENSP00000365543
HGNC28912
UniprotQ9Y484
UniprotA0A024QYW6

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0000045
IBA
Genome Projectautophagosome assembly
GO:0000422
IBA
Genome Projectmitophagy
GO:0006497
IBA
Genome Projectprotein lipidation
GO:0006914
IMP
IEA
Genome Projectautophagy
GO:0006995
IBA
Genome Projectcellular response to nitrogen starvation
GO:0034497
IBA
Genome Projectprotein localization to pre-autophagosomal structure
GO:0044804
IBA
Genome Projectnucleophagy

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0032266
IBA
Genome Projectphosphatidylinositol-3-phosphate binding
GO:0080025
IBA
Genome Projectphosphatidylinositol-3,5-bisphosphate binding

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005829
IBA
Genome Projectcytosol
GO:0019898
IBA
Genome Projectextrinsic component of membrane
GO:0034045
IBA
Genome Projectpre-autophagosomal structure membrane

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
Show redundant parents:  
 
InterPro Description
IPR001680WD40 repeat
IPR015943WD40/YVTN repeat-like-containing domain
IPR017986WD40-repeat-containing domain

No MapMan annotations defined for this gene.