EVI2B

EVI2B
Identifiers
AliasesEVI2B, CD361, D17S376, EVDB, ecotropic viral integration site 2B
External IDsMGI: 5439444 HomoloGene: 48438 GeneCards: EVI2B
Gene location (Human)
Chr.Chromosome 17 (human)[1]
Band17q11.2Start31,303,766 bp[1]
End31,314,112 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

2124

101488212

Ensembl

ENSG00000185862

ENSMUSG00000070354

UniProt

P34910

Q8VD58

RefSeq (mRNA)

NM_006495

NM_146023

RefSeq (protein)

NP_006486

NP_001070964

Location (UCSC)Chr 17: 31.3 – 31.31 MbChr 11: 79.51 – 79.53 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Protein EVI2B is a protein that in humans is encoded by the EVI2B gene.[5][6]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000185862 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000070354 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ Cawthon RM, Andersen LB, Buchberg AM, Xu GF, O'Connell P, Viskochil D, Weiss RB, Wallace MR, Marchuk DA, Culver M, et al. (Jun 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. doi:10.1016/0888-7543(91)90410-G. PMID 1903357.
  6. ↑ "Entrez Gene: EVI2B ecotropic viral integration site 2B".

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. doi:10.1016/0888-7543(92)90122-9. 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. PMC 359746. PMID 1899288.
  • 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. doi:10.1016/0092-8674(90)90253-B. 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. doi:10.1016/0888-7543(90)90199-5. 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. PMC 139241. 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. PMC 1356129. 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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