SLC35C1
From Wikipedia, the free encyclopedia
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Solute carrier family 35, member C1
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| Identifiers | ||||||||||||||
| Symbol(s) | SLC35C1; FLJ11320; FLJ14841; FUCT1 | |||||||||||||
| External IDs | OMIM: 605881 MGI: 2443301 HomoloGene: 41258 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 55343 | 228368 | ||||||||||||
| Ensembl | ENSG00000181830 | ENSMUSG00000049922 | ||||||||||||
| Uniprot | Q96A29 | n/a | ||||||||||||
| Refseq | NM_018389 (mRNA) NP_060859 (protein) |
NM_145832 (mRNA) NP_665831 (protein) |
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| Location | Chr 11: 45.78 - 45.79 Mb | Chr 2: 92.25 - 92.26 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
Solute carrier family 35, member C1, also known as SLC35C1, is a human gene.[1]
[edit] See also
[edit] References
[edit] Further reading
- 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. 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. PMID 9373149.
- Lühn K, Wild MK, Eckhardt M, et al. (2001). "The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter.". Nat. Genet. 28 (1): 69–72. doi:. PMID 11326279.
- Lübke T, Marquardt T, Etzioni A, et al. (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:. PMID 11326280.
- 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:. 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. doi:. 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:. 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:. 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:. PMID 16455955.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.

