| EVI2B | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | EVI2B, CD361, D17S376, EVDB, ecotropic viral integration site 2B | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 158381; MGI: 5439444; HomoloGene: 48438; GeneCards: EVI2B; OMA: EVI2B - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Protein EVI2B is a protein that in humans is encoded by the EVI2B gene. [5] [6]
- ^ a b c GRCh38: Ensembl release 89: ENSG00000185862 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070354 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ 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.
- ^ "Entrez Gene: EVI2B ecotropic viral integration site 2B".
- 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.
 | This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it. |
| EVI2B | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | EVI2B, CD361, D17S376, EVDB, ecotropic viral integration site 2B | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 158381; MGI: 5439444; HomoloGene: 48438; GeneCards: EVI2B; OMA: EVI2B - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Protein EVI2B is a protein that in humans is encoded by the EVI2B gene. [5] [6]
- ^ a b c GRCh38: Ensembl release 89: ENSG00000185862 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070354 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ 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.
- ^ "Entrez Gene: EVI2B ecotropic viral integration site 2B".
- 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.
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| This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it. |