GPM6B
From Wikipedia, the free encyclopedia
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Glycoprotein M6B
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| Identifiers | ||||||||||||||
| Symbol(s) | GPM6B; M6B; MGC17150; MGC54284 | |||||||||||||
| External IDs | OMIM: 300051 MGI: 107672 HomoloGene: 56966 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 2824 | 14758 | ||||||||||||
| Ensembl | ENSG00000046653 | ENSMUSG00000031342 | ||||||||||||
| Uniprot | Q13491 | Q3US81 | ||||||||||||
| Refseq | NM_001001994 (mRNA) NP_001001994 (protein) |
NM_023122 (mRNA) NP_075611 (protein) |
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| Location | Chr X: 13.7 - 13.75 Mb | Chr X: 161.58 - 161.73 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
Glycoprotein M6B, also known as GPM6B, is a human gene.[1]
[edit] References
[edit] Further reading
- Yan Y, Lagenaur C, Narayanan V (1993). "Molecular cloning of M6: identification of a PLP/DM20 gene family.". Neuron 11 (3): 423–31. PMID 8398137.
- Olinsky S, Loop BT, DeKosky A, et al. (1996). "Chromosomal mapping of the human M6 genes.". Genomics 33 (3): 532–6. doi:. PMID 8661015.
- Narayanan V, Olinsky S, Dahle E, et al. (1998). "Mutation analysis of the M6b gene in patients with Rett syndrome.". Am. J. Med. Genet. 78 (2): 165–8. PMID 9674909.
- Yoshida M, Shan WS, Colman DR (1999). "Conserved and divergent expression patterns of the proteolipid protein gene family in the amphibian central nervous system.". J. Neurosci. Res. 57 (1): 13–22. PMID 10397631.
- Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination.". Genome Res. 10 (11): 1788–95. PMID 11076863.
- Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.". Genome Res. 11 (3): 422–35. doi:. PMID 11230166.
- Werner H, Dimou L, Klugmann M, et al. (2002). "Multiple splice isoforms of proteolipid M6B in neurons and oligodendrocytes.". Mol. Cell. Neurosci. 18 (6): 593–605. doi:. PMID 11749036.
- 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:. PMID 12477932.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:. PMID 14702039.
- Henneke M, Wehner LE, Hennies HC, et al. (2005). "Mutation analysis of the M6b gene in patients with Pelizaeus-Merzbacher-like syndrome.". Am. J. Med. Genet. A 128 (2): 156–8. doi:. PMID 15214007.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:. PMID 15489334.
- Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline.". Genome Res. 14 (10B): 2136–44. doi:. PMID 15489336.
- Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006.". Nucleic Acids Res. 34 (Database issue): D415–8. doi:. PMID 16381901.

