SRPX2

From Wikipedia, the free encyclopedia


Sushi-repeat-containing protein, X-linked 2
Identifiers
Symbol(s) SRPX2; SRPX; SRPUL
External IDs MGI1916042 HomoloGene8704
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 27286 68792
Ensembl ENSG00000102359 ENSMUSG00000031253
Refseq NM_014467 (mRNA)
NP_055282 (protein)
NM_026838 (mRNA)
NP_081114 (protein)
Location Chr X: 99.79 - 99.81 Mb Chr X: 129.26 - 129.28 Mb
Pubmed search [1] [2]

Sushi-repeat-containing protein, X-linked 2, also known as SRPX2, is a human gene.[1]


[edit] References

[edit] Further reading

  • Kurosawa H, Goi K, Inukai T, et al. (1999). "Two candidate downstream target genes for E2A-HLF.". Blood 93 (1): 321–32. PMID 9864177. 
  • Suzuki Y, Taira H, Tsunoda T, et al. (2001). "Diverse transcriptional initiation revealed by fine, large-scale mapping of mRNA start sites.". EMBO Rep. 2 (5): 388–93. doi:10.1093/embo-reports/kve085. PMID 11375929. 
  • 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. 
  • Suzuki Y, Yamashita R, Shirota M, et al. (2004). "Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions.". Genome Res. 14 (9): 1711–8. doi:10.1101/gr.2435604. PMID 15342556. 
  • 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. PMID 15489334. 
  • Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature 434 (7031): 325–37. doi:10.1038/nature03440. PMID 15772651. 
  • 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:10.1093/dnares/12.2.117. PMID 16303743. 
  • Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMID 16344560. 
  • Roll P, Rudolf G, Pereira S, et al. (2006). "SRPX2 mutations in disorders of language cortex and cognition.". Hum. Mol. Genet. 15 (7): 1195–207. doi:10.1093/hmg/ddl035. PMID 16497722. 
  • Royer B, Soares DC, Barlow PN, et al. (2008). "Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas.". BMC Genet. 8: 72. doi:10.1186/1471-2156-8-72. PMID 17942002.