SLC7A10
From Wikipedia, the free encyclopedia
| Solute carrier family 7 (neutral amino acid transporter light chain, asc system), member 10 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||
| Symbols | SLC7A10; HASC-1; asc-1 | ||||||||||||
| External IDs | OMIM: 607959 MGI: 1858261 HomoloGene: 56767 GeneCards: SLC7A10 Gene | ||||||||||||
| |||||||||||||
| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 56301 | 53896 | |||||||||||
| Ensembl | ENSG00000130876 | ENSMUSG00000030495 | |||||||||||
| UniProt | Q9NS82 | P63115 | |||||||||||
| RefSeq (mRNA) | NM_019849 | NM_017394 | |||||||||||
| RefSeq (protein) | NP_062823 | NP_059090 | |||||||||||
| Location (UCSC) | Chr 19: 33.7 – 33.72 Mb | Chr 7: 35.19 – 35.2 Mb | |||||||||||
| PubMed search | |||||||||||||
Solute carrier family 7 member 10 also known as Asc-type amino acid transporter 1 or Asc-1 is a protein that in humans is encoded by the SLC7A10 gene.[1][2][3]
See also
- Heterodimeric amino acid transporter
References
- ↑ "Entrez Gene: solute carrier family 10".
- ↑ Fukasawa Y, Segawa H, Kim JY, Chairoungdua A, Kim DK, Matsuo H, Cha SH, Endou H, Kanai Y (March 2000). "Identification and characterization of a Na(+)-independent neutral amino acid transporter that associates with the 4F2 heavy chain and exhibits substrate selectivity for small neutral D- and L-amino acids". J. Biol. Chem. 275 (13): 9690–8. doi:10.1074/jbc.275.13.9690. PMID 10734121.
- ↑ Nakauchi J, Matsuo H, Kim DK, Goto A, Chairoungdua A, Cha SH, Inatomi J, Shiokawa Y, Yamaguchi K, Saito I, Endou H, Kanai Y (June 2000). "Cloning and characterization of a human brain Na(+)-independent transporter for small neutral amino acids that transports D-serine with high affinity". Neurosci. Lett. 287 (3): 231–5. doi:10.1016/S0304-3940(00)01169-1. PMID 10863037.
Further reading
- Leclerc D, Wu Q, Ellis JR, et al. (2001). "Is the SLC7A10 gene on chromosome 19 a candidate locus for cystinuria?". Mol. Genet. Metab. 73 (4): 333–9. doi:10.1006/mgme.2001.3209. PMID 11509015.
- Imielinski M, Baldassano RN, Griffiths A, et al. (2009). "Common variants at five new loci associated with early-onset inflammatory bowel disease.". Nat. Genet. 41 (12): 1335–40. doi:10.1038/ng.489. PMC 3267927. PMID 19915574.
- 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.
- Pineda M, Font M, Bassi MT, et al. (2004). "The amino acid transporter asc-1 is not involved in cystinuria.". Kidney Int. 66 (4): 1453–64. doi:10.1111/j.1523-1755.2004.00908.x. PMID 15458438.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "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:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Dehal P, Predki P, Olsen AS, et al. (2001). "Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution.". Science 293 (5527): 104–11. doi:10.1126/science.1060310. PMID 11441184.
- Bröer S (January 2008). "Amino acid transport across mammalian intestinal and renal epithelia". Physiol. Rev. 88 (1): 249–86. doi:10.1152/physrev.00018.2006. PMID 18195088.
- Xu D, Hemler ME (2005). "Metabolic activation-related CD147-CD98 complex.". Mol. Cell Proteomics 4 (8): 1061–71. doi:10.1074/mcp.M400207-MCP200. PMC 1351277. PMID 15901826.
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.