SLC35C1, solute carrier family 35 member C1

SLC35C1, solute carrier family 35 member C1

• This gene encodes a GDP-fucose transporter that is found in the Golgi apparatus. Mutations in this gene result in congenital disorder of glycosylation type IIc. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]

• Gene Synonyms (CDG2C, FUCT1, GDP-fucose transporter 1, solute carrier family 35 (GDP-fucose transporter), member C1,)
• NCBI Gene ID: 55343
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q96A29
  UNIPROT ID#>>B3KQH0
• 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.

solute carrier family 35 member C1 interacts with:

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.