MBNL3

From Wikipedia, the free encyclopedia

Muscleblind-like 3 (Drosophila)

Identifiers

MBNL3; CHCR; FLJ11316; MBLX; MBLX39; MBXL

External IDs

OMIM: 300413 MGI: 2444912 HomoloGene: 23101

Gene ontology
Molecular Function:	• nucleic acid binding • zinc ion binding • metal ion binding
Cellular Component:	• nucleus
Biological Process:	• multicellular organismal development • negative regulation of myoblast differentiation

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

Refseq

NM_018388 (mRNA)
NP_060858 (protein)

NM_134163 (mRNA)
NP_598924 (protein)

Location

Chr X: 131.33 - 131.45 Mb

Chr X: 47.37 - 47.41 Mb

Pubmed search

[1]

[2]

Muscleblind-like 3 (Drosophila), also known as MBNL3, is a human gene.^[1]

[edit] References

^ Entrez Gene: MBNL3 muscleblind-like 3 (Drosophila).

[edit] Further reading

Miller JW, Urbinati CR, Teng-Umnuay P, et al. (2000). "Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy.". EMBO J. 19 (17): 4439-48. doi:10.1093/emboj/19.17.4439. PMID 10970838.
Fardaei M, Rogers MT, Thorpe HM, et al. (2002). "Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.". Hum. Mol. Genet. 11 (7): 805-14. PMID 11929853.
Squillace RM, Chenault DM, Wang EH (2002). "Inhibition of muscle differentiation by the novel muscleblind-related protein CHCR.". Dev. Biol. 250 (1): 218-30. PMID 12297108.
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. 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:10.1038/ng1285. PMID 14702039.
Ho TH, Charlet-B N, Poulos MG, et al. (2005). "Muscleblind proteins regulate alternative splicing.". EMBO J. 23 (15): 3103-12. doi:10.1038/sj.emboj.7600300. PMID 15257297.
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:10.1101/gr.2596504. PMID 15489334.
Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature 434 (7031): 325-37. doi:10.1038/nature03440. PMID 15772651.
Self JE, Ennis S, Collins A, et al. (2006). "Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.". Mol. Vis. 12: 1211-6. PMID 17102799.