Gene: ENSG00000148584 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000148584
Transcript Identifier
ENST00000395489
Gene Type
Coding gene
Location
10 : 50806729-50850787 : negative

Family Information

Homologous gene family
HOM03P001632
(47 genes in 18 species)
specific family
Orthologous gene family
ORTHO03P064980
(2 genes in 2 species)
specific family

Descriptions

gene_descr
APOBEC1 complementation factor

Identifiers

Type Value
pidENSP00000378868
HGNC24086
UniprotF8W9F8

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0010609
IEA
Genome ProjectmRNA localization resulting in posttranscriptional regulation of gene expression
GO:0016554
IEA
Genome Projectcytidine to uridine editing
GO:0016556
IEA
Genome ProjectmRNA modification

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0000166
IEA
Genome Projectnucleotide binding
GO:0003676
IEA
Genome Projectnucleic acid binding
GO:0003729
IEA
Genome ProjectmRNA binding

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005634
IEA
Genome Projectnucleus
GO:0005654
IDA
Genome Projectnucleoplasm
GO:0005720
IEA
Genome Projectnuclear heterochromatin
GO:0005737
IEA
Genome Projectcytoplasm
GO:0045293
IEA
Genome ProjectmRNA editing complex

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
Show redundant parents:  
 
InterPro Description
IPR000504RNA recognition motif domain
IPR006535HnRNP R/Q splicing factor
IPR012677Nucleotide-binding alpha-beta plait domain
IPR014720Double-stranded RNA-binding domain

No MapMan annotations defined for this gene.