TMEM199, transmembrane protein 199

TMEM199, transmembrane protein 199

• The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) in some human cells. The encoded protein shares some homology with the yeast protein Vma12. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. [provided by RefSeq, Mar 2016]

• Gene Synonyms (C17orf32, CDG2P, VMA12, VPH2, transmembrane protein 199,)
• NCBI Gene ID: 147007
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q8N511
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

transmembrane protein 199 interacts with:

• ATPase H+ transporting V0 subunit d2
  KASH domain containing 5
  solute carrier family 10 member 4
  transmembrane protein 17
  vacuolar ATPase assembly factor VMA21

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.