Human (GRCh38.p14)
Description

component of oligomeric golgi complex 7 [Source:HGNC Symbol;Acc:HGNC:18622]

Location

Chromosome 16: 23,388,493-23,453,189 reverse strand.

GRCh38:CM000678.2

About this gene

This gene has 6 transcripts (splice variants), 208 orthologues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000307149.10COG7-2012935770aaENSP00000305442.5
 
Protein coding
CCDS10610A0A0S2Z652 P83436 NM_153603.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000563164.1COG7-203741113aaENSP00000460151.1
 
Protein coding
I3L337 -TSL:3CDS 5' incomplete
ENST00000561854.1COG7-20281488aaENSP00000459872.1
 
Nonsense mediated decay
I3L2R8 -TSL:3CDS 5' incomplete
ENST00000569635.1COG7-206474No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000566364.1COG7-204939No protein-
 
Retained intron
--TSL:2
ENST00000567821.1COG7-205922No protein-
 
Retained intron
--TSL:5