Human (GRCh38.p14)
Description

C-X9-C motif containing 1 [Source:HGNC Symbol;Acc:HGNC:28783]

Gene Synonyms

C3ORF68, MGC61571

Location

Chromosome 3: 28,241,584-28,325,142 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 11 transcripts (splice variants) and 127 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000466830.6CMC1-2056009106aaENSP00000418348.1
 
Protein coding
CCDS33722Q7Z7K0 NM_182523.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000423894.5CMC1-20454976aaENSP00000404581.1
 
Protein coding
CCDS87055C9JES7 -GENCODE basicTSL:2
ENST00000334841.10CMC1-20172447aaENSP00000334960.6
 
Nonsense mediated decay
F8WAC1 -TSL:3
ENST00000469102.1CMC1-208788No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000418849.2CMC1-203670No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000495428.5CMC1-211608No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000468330.1CMC1-207551No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000467644.5CMC1-206549No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000482499.1CMC1-210446No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000477739.1CMC1-2093749No protein-
 
Retained intron
--TSL:1
ENST00000396610.6CMC1-202593No protein-
 
Retained intron
--TSL:2