Gene: ENSG00000135297 (Homo sapiens)

Overview top

Gene Identifier
ENSG00000135297
Transcript Identifier
ENST00000415954
Gene Type
Coding gene
Location
6 : 73461855-73500735 : positive

Family Information

Homologous gene family
HOM03P001323
(53 genes in 37 species)
specific family
Orthologous gene family
ORTHO03P002510
(30 genes in 30 species)
specific family

Descriptions

gene_descr
mitochondrial tRNA translation optimization 1

Identifiers

Type Value
pidENSP00000402038
HGNC19261
UniprotQ9Y2Z2

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Biological Process

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0002098
IEA
Genome ProjecttRNA wobble uridine modification
GO:0008033
IEA
Genome ProjecttRNA processing
GO:0070899
IEA
Genome Projectmitochondrial tRNA wobble uridine modification

Molecular Function

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0044822
IDA
Genome Projectpoly(A) RNA binding
GO:0050660
IEA
Genome Projectflavin adenine dinucleotide binding

Cellular Component

GO termEvidence(s)Provider(s)DescriptionSource(s)
GO:0005739
IEA
Genome Projectmitochondrion

Color Legend

Experimental Evidence
Computational Reviewed Evidence
Electronic Evidence
GO Sources:   Primary     Orthology     Homology  
Show redundant parents:  
 
InterPro Description
IPR002218tRNA uridine 5-carboxymethylaminomethyl modification enzyme MnmG-related
IPR020595MnmG-related, conserved site
IPR023753FAD/NAD(P)-binding domain
IPR026904GidA associated domain 3

No MapMan annotations defined for this gene.