Human (GRCh38.p14)
Description

cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 [Source:HGNC Symbol;Acc:HGNC:2260]

Location

Chromosome 17: 14,069,490-14,231,736 forward strand.

GRCh38:CM000679.2

About this gene

This gene has 7 transcripts (splice variants), 199 orthologues, 1 paralogue and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000261643.8COX10-2012898443aaENSP00000261643.3
 
Protein coding
CCDS11166Q12887-1 NM_001303.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000429152.6COX10-202875171aaENSP00000397750.2
 
Protein coding
H7C101 -GENCODE basicTSL:2
ENST00000664217.1COX10-2064948443aaENSP00000499396.1
 
Nonsense mediated decay
CCDS11166Q12887-1 --
ENST00000670279.1COX10-2073180315aaENSP00000499450.1
 
Nonsense mediated decay
A0A590UJJ5 --
ENST00000581931.5COX10-2051509168aaENSP00000462512.1
 
Nonsense mediated decay
J3KSJ3 -TSL:2
ENST00000580561.1COX10-204138462aaENSP00000462190.1
 
Nonsense mediated decay
J3KRW4 -TSL:2
ENST00000458492.1COX10-2031537No protein-
 
Protein coding CDS not defined
--TSL:1