Disease-gene associations mined from literature

Literature associating COG4 and congenital disorder of glycosylation type IIe

COG4 [ENSP00000315775]

Conserved oligomeric Golgi complex subunit 4; Required for normal Golgi function. Plays a role in SNARE-pin assembly and Golgi-to-ER retrograde transport via its interaction with SCFD1; Belongs to the COG4 family.

Synonyms:  COG4,  COG4p,  hCOG4,  B4DDL2,  COG4-001 ...

Linkouts:  STRING  Pharos  UniProt  OMIM