SLC35C1

SLC35C1
Identifiers
Aliases SLC35C1, CDG2C, FUCT1, solute carrier family 35 member C1
External IDs MGI: 2443301 HomoloGene: 41258 GeneCards: SLC35C1
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

55343

228368

Ensembl

ENSG00000181830

ENSMUSG00000049922

UniProt

Q96A29

Q8BLX4

RefSeq (mRNA)

NM_001145265
NM_001145266
NM_018389

NM_145832
NM_211358

RefSeq (protein)

NP_001138737.1
NP_001138738.1
NP_060859.4

NP_997597.1

Location (UCSC) Chr 11: 45.8 – 45.81 Mb Chr 2: 92.45 – 92.46 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

GDP-fucose transporter 1 is a protein that in humans is encoded by the SLC35C1 gene.[3][4][5]

Defects can be associated with Congenital disorder of glycosylation type IIc.

See also

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. Luhn K, Wild MK, Eckhardt M, Gerardy-Schahn R, Vestweber D (Apr 2001). "The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter". Nat Genet. 28 (1): 69–72. doi:10.1038/88289. PMID 11326279.
  4. Lubke T, Marquardt T, Etzioni A, Hartmann E, von Figura K, Korner C (Apr 2001). "Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as a GDP-fucose transporter deficiency". Nat Genet. 28 (1): 73–6. doi:10.1038/88299. PMID 11326280.
  5. "Entrez Gene: SLC35C1 solute carrier family 35, member C1".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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