EVI2B

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

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 79,513,385 bp[2] End 79,530,589 bp[2]
RNA expression pattern 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: 79.51 – 79.53 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

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. 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. 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.