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GDP-fucose transporter 1

From Wikipedia, the free encyclopedia
SLC35C1
Identifiers
AliasesSLC35C1, CDG2C, FUCT1, solute carrier family 35 member C1
External IDsOMIM: 605881; MGI: 2443301; HomoloGene: 41258; GeneCards: SLC35C1; OMA:SLC35C1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001145265
NM_001145266
NM_018389

NM_145832
NM_211358

RefSeq (protein)

NP_001138737
NP_001138738
NP_060859

NP_665831
NP_997597

Location (UCSC)Chr 11: 45.8 – 45.81 MbChr 2: 92.28 – 92.29 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

GDP-fucose transporter 1 is a protein that in humans is encoded by the SLC35C1 gene.[5][6][7]

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

See also

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000181830Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049922Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ 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.
  6. ^ 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.
  7. ^ "Entrez Gene: SLC35C1 solute carrier family 35, member C1".

Further reading

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