NIPA2

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Non imprinted in Prader-Willi/Angelman syndrome 2
Identifiers
Symbol(s) NIPA2; MGC5466
External IDs OMIM: 608146 MGI: 1913918 HomoloGene: 11368
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 81614 93790
Ensembl ENSG00000140157 ENSMUSG00000030452
Uniprot Q8N8Q9 Q921M1
Refseq NM_001008860 (mRNA)
NP_001008860 (protein)		 NM_023647 (mRNA)
NP_076136 (protein)
Location Chr 15: 20.56 - 20.59 Mb Chr 7: 55.8 - 55.83 Mb
Pubmed search [1] [2]

Non imprinted in Prader-Willi/Angelman syndrome 2, also known as NIPA2, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: NIPA2 non imprinted in Prader-Willi/Angelman syndrome 2.

[edit] Further reading

  • Bittel DC, Kibiryeva N, Butler MG (2006). "Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.". Pediatrics 118 (4): e1276-83. doi:10.1542/peds.2006-0424. PMID 16982806. 
  • 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. 
  • Lefèvre C, Bouadjar B, Karaduman A, et al. (2005). "Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis.". Hum. Mol. Genet. 13 (20): 2473-82. doi:10.1093/hmg/ddh263. PMID 15317751. 
  • Glinsky GV, Glinskii AB, Stephenson AJ, et al. (2004). "Gene expression profiling predicts clinical outcome of prostate cancer.". J. Clin. Invest. 113 (6): 913-23. doi:10.1172/JCI20032. PMID 15067324. 
  • 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. 
  • Chai JH, Locke DP, Greally JM, et al. (2003). "Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.". Am. J. Hum. Genet. 73 (4): 898-925. PMID 14508708. 
  • 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. 
  • Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction.". Anal. Biochem. 236 (1): 107-13. doi:10.1006/abio.1996.0138. PMID 8619474. 
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