MASTL

From Wikipedia, the free encyclopedia


Microtubule associated serine/threonine kinase-like
Identifiers
Symbol(s) MASTL; FLJ14813; RP11-85G18.2; THC2
External IDs OMIM: 608221 MGI: 1914371 HomoloGene: 12086
Orthologs
Human Mouse
Entrez 84930 67121
Ensembl ENSG00000120539 ENSMUSG00000026779
Uniprot Q96GX5 Q3MIA9
Refseq NM_032844 (mRNA)
NP_116233 (protein)		 NM_025979 (mRNA)
NP_080255 (protein)
Location Chr 10: 27.48 - 27.52 Mb Chr 2: 22.94 - 22.98 Mb
Pubmed search [1] [2]

Microtubule associated serine/threonine kinase-like, also known as MASTL, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: MASTL microtubule associated serine/threonine kinase-like.

[edit] Further reading

  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171–4. PMID 8125298. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149–56. PMID 9373149. 
  • Savoia A, Del Vecchio M, Totaro A, et al. (1999). "An autosomal dominant thrombocytopenia gene maps to chromosomal region 10p.". Am. J. Hum. Genet. 65 (5): 1401–5. PMID 10521306. 
  • Drachman JG, Jarvik GP, Mehaffey MG (2000). "Autosomal dominant thrombocytopenia: incomplete megakaryocyte differentiation and linkage to human chromosome 10.". Blood 96 (1): 118–25. PMID 10891439. 
  • 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. 
  • Gandhi MJ, Cummings CL, Drachman JG (2004). "FLJ14813 missense mutation: a candidate for autosomal dominant thrombocytopenia on human chromosome 10.". Hum. Hered. 55 (1): 66–70. doi:10.1159/000071812. PMID 12890928. 
  • 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. 
  • Deloukas P, Earthrowl ME, Grafham DV, et al. (2004). "The DNA sequence and comparative analysis of human chromosome 10.". Nature 429 (6990): 375–81. doi:10.1038/nature02462. PMID 15164054. 
  • 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. 
  • Beausoleil SA, Villén J, Gerber SA, et al. (2006). "A probability-based approach for high-throughput protein phosphorylation analysis and site localization.". Nat. Biotechnol. 24 (10): 1285–92. doi:10.1038/nbt1240. PMID 16964243. 
 This article on a gene on chromosome 10 is a stub. You can help Wikipedia by expanding it.