EVI2B

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Ecotropic viral integration site 2B
Identifiers
Symbol(s) EVI2B; D17S376; EVDB
External IDs OMIM: 158381 MGI: 1890682 HomoloGene: 48438
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 2124 216984
Ensembl ENSG00000185862 n/a
Uniprot P34910 n/a
Refseq NM_006495 (mRNA)
NP_006486 (protein)		 NM_001077496 (mRNA)
NP_001070964 (protein)
Location Chr 17: 26.65 - 26.67 Mb n/a
Pubmed search [1] [2]

Ecotropic viral integration site 2B, also known as EVI2B, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: EVI2B ecotropic viral integration site 2B.

[edit] Further reading

  • Xu G, O'Connell P, Stevens J, White R (1992). "Characterization of human adenylate kinase 3 (AK3) cDNA and mapping of the AK3 pseudogene to an intron of the NF1 gene.". Genomics 13 (3): 537–42. PMID 1639383. 
  • Wallace MR, Andersen LB, Saulino AM, et al. (1991). "A de novo Alu insertion results in neurofibromatosis type 1.". Nature 353 (6347): 864–6. doi:10.1038/353864a0. PMID 1719426. 
  • Viskochil D, Cawthon R, O'Connell P, et al. (1991). "The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene.". Mol. Cell. Biol. 11 (2): 906–12. PMID 1899288. 
  • Cawthon RM, Andersen LB, Buchberg AM, et al. (1991). "cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene.". Genomics 9 (3): 446–60. PMID 1903357. 
  • Cawthon RM, Weiss R, Xu GF, et al. (1990). "A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations.". Cell 62 (1): 193–201. PMID 2114220. 
  • Cawthon RM, O'Connell P, Buchberg AM, et al. (1990). "Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts.". Genomics 7 (4): 555–65. PMID 2117566. 
  • 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. 
  • 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. 
  • Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.". Nat. Genet. 39 (8): 963–5. doi:10.1038/ng2083. PMID 17632510. 
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