EVI2B

EVI2B
Identifiers
Aliases	EVI2B , CD361, D17S376, EVDB, ecotropic viral integration site 2B
External IDs	OMIM: 158381 MGI: 5439444 HomoloGene: 48438 GeneCards: EVI2B
Gene location (Human) Chr. Chromosome 17 (human) [1] Band 17q11.2 Start 31,303,770 bp [1] End 31,314,105 bp [1]
Gene location (Mouse) Chr. Chromosome 11 (mouse) [2] Band 11 B5|11 Start 79,404,211 bp [2] End 79,421,415 bp [2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in monocyte blood bone marrow bone marrow cells cancellous bone spleen appendix lymph node right lung lower lobe of lung Top expressed in bone marrow blood thymus spleen aortic valve lip esophagus jejunum duodenum neural tube More reference expression data BioGPS More reference expression data
Orthologs Species Human Mouse Entrez 2124 101488212 Ensembl ENSG00000185862 ENSMUSG00000070354 UniProt P34910 Q8VD58 RefSeq (mRNA) NM_006495 NM_146023 RefSeq (protein) NP_006486 NP_666135 NP_001070964 Location (UCSC) Chr 17: 31.3 – 31.31 Mb Chr 11: 79.4 – 79.42 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

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

References

1. GRCh38: Ensembl release 89: ENSG00000185862 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000070354 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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. hdl: 2027.42/29439 . 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" (PDF). Nature. 353 (6347): 864–6. Bibcode:1991Natur.353..864W. doi:10.1038/353864a0. hdl: 2027.42/62641 . PMID   1719426. S2CID   4309841.
• 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. doi:10.1128/mcb.11.2.906. 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. S2CID   8201518.
• 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. Bibcode:2002PNAS...9916899M. 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. S2CID   35797973.