SEMA4F
From Wikipedia, the free encyclopedia
Sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F
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Identifiers | ||||||||||||||
Symbol(s) | SEMA4F; M-SEMA; PRO2353; SEMAM; SEMAW; m-Sema M; m-Sema-M | |||||||||||||
External IDs | OMIM: 603706 MGI: 1340055 HomoloGene: 3147 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 10505 | 20355 | ||||||||||||
Ensembl | ENSG00000135622 | ENSMUSG00000000627 | ||||||||||||
Uniprot | O95754 | Q505G0 | ||||||||||||
Refseq | NM_004263 (mRNA) NP_004254 (protein) |
NM_011350 (mRNA) NP_035480 (protein) |
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Location | Chr 2: 74.73 - 74.76 Mb | Chr 6: 82.88 - 82.91 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F, also known as SEMA4F, is a human gene.[1]
[edit] References
[edit] Further reading
- Giger RJ, Urquhart ER, Gillespie SK, et al. (1999). "Neuropilin-2 is a receptor for semaphorin IV: insight into the structural basis of receptor function and specificity.". Neuron 21 (5): 1079–92. PMID 9856463.
- Encinas JA, Kikuchi K, Chedotal A, et al. (1999). "Cloning, expression, and genetic mapping of Sema W, a member of the semaphorin family.". Proc. Natl. Acad. Sci. U.S.A. 96 (5): 2491–6. PMID 10051670.
- Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination.". Genome Res. 10 (11): 1788–95. PMID 11076863.
- Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.". Genome Res. 11 (3): 422–35. doi: . PMID 11230166.
- Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing.". EMBO Rep. 1 (3): 287–92. doi: . PMID 11256614.
- Schultze W, Eulenburg V, Lessmann V, et al. (2001). "Semaphorin4F interacts with the synapse-associated protein SAP90/PSD-95.". J. Neurochem. 78 (3): 482–9. PMID 11483650.
- Francks C, Fisher SE, Olson RK, et al. (2002). "Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.". Psychiatr. Genet. 12 (1): 35–41. PMID 11901358.
- 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.
- 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.
- Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline.". Genome Res. 14 (10B): 2136–44. doi: . PMID 15489336.
- Hillier LW, Graves TA, Fulton RS, et al. (2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4.". Nature 434 (7034): 724–31. doi: . PMID 15815621.
- Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.". DNA Res. 12 (2): 117–26. doi: . PMID 16303743.
- Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006.". Nucleic Acids Res. 34 (Database issue): D415–8. doi: . PMID 16381901.