KIAA0196

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KIAA0196
Identifiers
Symbol(s) KIAA0196; MGC111053; SPG8
External IDs OMIM: 610657 MGI: 2146110 HomoloGene: 8898
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 9897 223593
Ensembl ENSG00000164961 ENSMUSG00000022350
Uniprot Q12768 Q3TQ26
Refseq NM_014846 (mRNA)
NP_055661 (protein)		 NM_153548 (mRNA)
NP_705776 (protein)
Location Chr 8: 126.11 - 126.17 Mb Chr 15: 59.16 - 59.2 Mb
Pubmed search [1] [2]

KIAA0196 is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: KIAA0196 KIAA0196.

[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. 
  • Nagase T, Seki N, Ishikawa K, et al. (1996). "Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1.". DNA Res. 3 (1): 17–24. PMID 8724849. 
  • 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. 
  • Hedera P, Rainier S, Alvarado D, et al. (1999). "Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.". Am. J. Hum. Genet. 64 (2): 563–9. PMID 9973294. 
  • 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. 
  • Gevaert K, Goethals M, Martens L, et al. (2004). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides.". Nat. Biotechnol. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801. 
  • Porkka KP, Tammela TL, Vessella RL, Visakorpi T (2004). "RAD21 and KIAA0196 at 8q24 are amplified and overexpressed in prostate cancer.". Genes Chromosomes Cancer 39 (1): 1–10. doi:10.1002/gcc.10289. PMID 14603436. 
  • 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. 
  • 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. 
  • Valdmanis PN, Meijer IA, Reynolds A, et al. (2007). "Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.". Am. J. Hum. Genet. 80 (1): 152–61. doi:10.1086/510782. PMID 17160902. 
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