LIN7C

From Wikipedia, the free encyclopedia


Lin-7 homolog C (C. elegans)
PDB rendering based on 2dkr.
Available structures: 2dkr
Identifiers
Symbol(s) LIN7C; FLJ11215; LIN-7-C; LIN-7C; MALS-3; VELI3
External IDs MGI1330839 HomoloGene22649
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 55327 22343
Ensembl ENSG00000148943 ENSMUSG00000027162
Uniprot Q9NUP9 Q3TS99
Refseq NM_018362 (mRNA)
NP_060832 (protein)
NM_011699 (mRNA)
NP_035829 (protein)
Location Chr 11: 27.47 - 27.48 Mb Chr 2: 109.69 - 109.7 Mb
Pubmed search [1] [2]

Lin-7 homolog C (C. elegans), also known as LIN7C, is a human gene.[1]


[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. 
  • Jo K, Derin R, Li M, Bredt DS (1999). "Characterization of MALS/Velis-1, -2, and -3: a family of mammalian LIN-7 homologs enriched at brain synapses in association with the postsynaptic density-95/NMDA receptor postsynaptic complex.". J. Neurosci. 19 (11): 4189–99. PMID 10341223. 
  • Bécamel C, Alonso G, Galéotti N, et al. (2002). "Synaptic multiprotein complexes associated with 5-HT(2C) receptors: a proteomic approach.". EMBO J. 21 (10): 2332–42. doi:10.1093/emboj/21.10.2332. PMID 12006486. 
  • 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:10.1073/pnas.242603899. PMID 12477932. 
  • Hori K, Konno D, Maruoka H, Sobue K (2003). "MALS is a binding partner of IRSp53 at cell-cell contacts.". FEBS Lett. 554 (1-2): 30–4. PMID 14596909. 
  • 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. 
  • Leonoudakis D, Conti LR, Radeke CM, et al. (2004). "A multiprotein trafficking complex composed of SAP97, CASK, Veli, and Mint1 is associated with inward rectifier Kir2 potassium channels.". J. Biol. Chem. 279 (18): 19051–63. doi:10.1074/jbc.M400284200. PMID 14960569. 
  • Leonoudakis D, Conti LR, Anderson S, et al. (2004). "Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins.". J. Biol. Chem. 279 (21): 22331–46. doi:10.1074/jbc.M400285200. PMID 15024025. 
  • Petrosky KY, Ou HD, Löhr F, et al. (2006). "A general model for preferential hetero-oligomerization of LIN-2/7 domains: mechanism underlying directed assembly of supramolecular signaling complexes.". J. Biol. Chem. 280 (46): 38528–36. doi:10.1074/jbc.M506536200. PMID 16147993. 
  • Mendes CC, Gomes DA, Thompson M, et al. (2006). "The type III inositol 1,4,5-trisphosphate receptor preferentially transmits apoptotic Ca2+ signals into mitochondria.". J. Biol. Chem. 280 (49): 40892–900. doi:10.1074/jbc.M506623200. PMID 16192275. 
  • Bohl J, Brimer N, Lyons C, Vande Pol SB (2007). "The stardust family protein MPP7 forms a tripartite complex with LIN7 and DLG1 that regulates the stability and localization of DLG1 to cell junctions.". J. Biol. Chem. 282 (13): 9392–400. doi:10.1074/jbc.M610002200. PMID 17237226. 
  • Onda T, Uzawa K, Nakashima D, et al. (2007). "Lin-7C/VELI3/MALS-3: an essential component in metastasis of human squamous cell carcinoma.". Cancer Res. 67 (20): 9643–8. doi:10.1158/0008-5472.CAN-07-1911. PMID 17942893.