Human (GRCh38.p14)
Description

mitochondrial calcium uniporter [Source:HGNC Symbol;Acc:HGNC:23526]

Gene Synonyms

C10ORF42, CCDC109A, FLJ46135

Location

Chromosome 10: 72,692,143-72,887,694 forward strand.

GRCh38:CM000672.2

About this gene

This gene has 11 transcripts (splice variants), 205 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000373053.8MCU-2022937351aaENSP00000362144.3
 
Protein coding
CCDS7317Q8NE86-1 NM_138357.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000536019.5MCU-2043224302aaENSP00000440913.1
 
Protein coding
CCDS59219Q8NE86-3 -GENCODE basicTSL:2
ENST00000357157.10MCU-2012874330aaENSP00000349680.6
 
Protein coding
CCDS59218Q8NE86-2 -GENCODE basicTSL:1
ENST00000604152.1MCU-207556167aaENSP00000475141.1
 
Protein coding
S4R468 -TSL:5CDS 3' incomplete
ENST00000605597.5MCU-211322488aaENSP00000473892.1
 
Nonsense mediated decay
S4R332 -TSL:2
ENST00000604679.5MCU-2091074101aaENSP00000473857.1
 
Nonsense mediated decay
S4R319 -TSL:5
ENST00000604372.5MCU-20889454aaENSP00000474820.1
 
Nonsense mediated decay
S4R3W8 -TSL:1
ENST00000603649.5MCU-20647391aaENSP00000474265.1
 
Nonsense mediated decay
S4R3F5 -TSL:5
ENST00000605416.1MCU-2102288No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000603118.5MCU-205544No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000483185.1MCU-203637No protein-
 
Retained intron
--TSL:3