KIAA1199

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KIAA1199
Identifiers
Symbol(s) KIAA1199; TMEM2L
External IDs OMIM: 608366 MGI: 2443629 HomoloGene: 10268
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 57214 80982
Ensembl ENSG00000103888 ENSMUSG00000052353
Uniprot Q8WUJ3 Q14AX8
Refseq NM_018689 (mRNA)
NP_061159 (protein)		 NM_030728 (mRNA)
NP_109653 (protein)
Location Chr 15: 78.86 - 79.03 Mb Chr 7: 83.81 - 83.96 Mb
Pubmed search [1] [2]

KIAA1199, also known as KIAA1199, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: KIAA1199 KIAA1199.

[edit] Further reading

  • Nagase T, Ishikawa K, Kikuno R, et al. (2000). "Prediction of the coding sequences of unidentified human genes. XV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.". DNA Res. 6 (5): 337-45. PMID 10574462. 
  • Wines ME, Lee L, Katari MS, et al. (2001). "Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysis.". Genomics 72 (1): 88-98. doi:10.1006/geno.2000.6466. PMID 11247670. 
  • Nakayama M, Kikuno R, Ohara O (2003). "Protein-protein interactions between large proteins: two-hybrid screening using a functionally classified library composed of long cDNAs.". Genome Res. 12 (11): 1773-84. doi:10.1101/gr.406902. PMID 12421765. 
  • Abe S, Katagiri T, Saito-Hisaminato A, et al. (2003). "Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues.". Am. J. Hum. Genet. 72 (1): 73-82. PMID 12471561. 
  • 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. 
  • Abe S, Usami S, Nakamura Y (2004). "Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss.". J. Hum. Genet. 48 (11): 564-70. doi:10.1007/s10038-003-0079-2. PMID 14577002. 
  • 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. 
  • Michishita E, Garcés G, Barrett JC, Horikawa I (2006). "Upregulation of the KIAA1199 gene is associated with cellular mortality.". Cancer Lett. 239 (1): 71-7. doi:10.1016/j.canlet.2005.07.028. PMID 16157444. 
  • Guo J, Cheng H, Zhao S, Yu L (2006). "GG: a domain involved in phage LTF apparatus and implicated in human MEB and non-syndromic hearing loss diseases.". FEBS Lett. 580 (2): 581-4. doi:10.1016/j.febslet.2005.12.076. PMID 16406369. 
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