Protein-coding gene in the species Homo sapiens
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.
- ^ a b c GRCh38: Ensembl release 89: ENSG00000181830 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049922 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ 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.
- ^ 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.
- ^ "Entrez Gene: SLC35C1 solute carrier family 35, member C1".
- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Hidalgo A, Ma S, Peired AJ, et al. (2003). "Insights into leukocyte adhesion deficiency type 2 from a novel mutation in the GDP-fucose transporter gene". Blood. 101 (5): 1705–12. doi:10.1182/blood-2002-09-2840. PMID 12406889.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Helmus Y, Denecke J, Yakubenia S, et al. (2006). "Leukocyte adhesion deficiency II patients with a dual defect of the GDP-fucose transporter". Blood. 107 (10): 3959–66. doi:10.1182/blood-2005-08-3334. PMID 16455955.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
|
|---|
By group |
|---|
SLC1–10 |
|---|
| (1): | |
|---|
| (2): | |
|---|
| (3): | |
|---|
| (4): | |
|---|
| (5): | |
|---|
| (6): | |
|---|
| (7): | |
|---|
| (8): | |
|---|
| (9): | |
|---|
| (10): | |
|---|
|
| SLC11–20 |
|---|
| (11): | |
|---|
| (12): | |
|---|
| (13): | |
|---|
| (14): | |
|---|
| (15): | |
|---|
| (16): | |
|---|
| (17): | |
|---|
| (18): | |
|---|
| (19): | |
|---|
| (20): | |
|---|
|
| SLC21–30 |
|---|
| (21): | |
|---|
| (22): | |
|---|
| (23): | |
|---|
| (24): | |
|---|
| (25): | |
|---|
| (26): | |
|---|
| (27): | |
|---|
| (28): | |
|---|
| (29): | |
|---|
| (30): | |
|---|
|
| SLC31–40 |
|---|
| (31): | |
|---|
| (32): | |
|---|
| (33): | |
|---|
| (34): | |
|---|
| (35): | |
|---|
| (36): | |
|---|
| (37): | |
|---|
| (38): | |
|---|
| (39): | |
|---|
| (40): | |
|---|
|
| SLC41–48 |
|---|
| (41): | |
|---|
| (42): | |
|---|
| (43): | |
|---|
| (44): | |
|---|
| (45): | |
|---|
| (46): | |
|---|
| (47): | |
|---|
| (48): | |
|---|
|
| |
|
|
|
|
