Gene: ENSG00000137288 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000137288
Transcript Identifier
ENST00000607484
Gene Type
Coding gene
Location
6 : 33697653-33711686 : negative

Family Information

Homologous gene family
HOM03P059283
(orphan gene)
specific family

Descriptions

gene_descr
ubiquinol-cytochrome c reductase complex assembly factor 2

Identifiers

Type Value
pidENSP00000476140
HGNC21237
UniprotQ9BRT2

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0002082
IMP
Genome Projectregulation of oxidative phosphorylation
GO:0034551
IDA
Genome Projectmitochondrial respiratory chain complex III assembly
GO:0050796
ISS
IEA
Genome Projectregulation of insulin secretion
GO:0070131
IDA
Genome Projectpositive regulation of mitochondrial translation
GO:1903364
IMP
Genome Projectpositive regulation of cellular protein catabolic process
GO:2001014
ISS
IEA
Genome Projectregulation of skeletal muscle cell differentiation

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005515
IPI
Genome Projectprotein binding

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005634
IDA
Genome Projectnucleus
GO:0005739
IDA
IEA
Genome Projectmitochondrion
GO:0005743
ISS
IEA
Genome Projectmitochondrial inner membrane
GO:0005758
ISS
IEA
Genome Projectmitochondrial intermembrane space
GO:0005759
ISS
IEA
Genome Projectmitochondrial matrix
GO:0016020
IEA
Genome Projectmembrane
GO:0042645
IDA
IEA
Genome Projectmitochondrial nucleoid

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
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No InterPro domains detected for this gene.
No MapMan annotations defined for this gene.