TMEM112

From Wikipedia, the free encyclopedia


Transmembrane protein 112
Identifiers
Symbol(s) TMEM112; C16orf26; FLJ12681; FLJ22302; HMFN1876; JFP11; TMEM112A
External IDs MGI: 1923733 HomoloGene: 23384
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 64788 76483
Ensembl ENSG00000103227 ENSMUSG00000002279
Refseq NM_022773 (mRNA)
NP_073610 (protein)		 NM_029624 (mRNA)
NP_083900 (protein)
Location Chr 16: 0.84 - 0.96 Mb Chr 17: 25.31 - 25.39 Mb
Pubmed search [1] [2]

Transmembrane protein 112, also known as TMEM112, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: TMEM112 transmembrane protein 112.

[edit] Further reading

  • Péterfy M, Ben-Zeev O, Mao HZ, et al. (2007). "Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia.". Nat. Genet. 39 (12): 1483-7. doi:10.1038/ng.2007.24. PMID 17994020. 
  • 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. PMID 16344560. 
  • 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. 
  • Yamada S, Ohira M, Horie H, et al. (2004). "Expression profiling and differential screening between hepatoblastomas and the corresponding normal livers: identification of high expression of the PLK1 oncogene as a poor-prognostic indicator of hepatoblastomas.". Oncogene 23 (35): 5901-11. doi:10.1038/sj.onc.1207782. PMID 15221005. 
  • 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. 
  • 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. 
  • Daniels RJ, Peden JF, Lloyd C, et al. (2001). "Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16.". Hum. Mol. Genet. 10 (4): 339-52. PMID 11157797. 
  • 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. 
  • 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. 
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