Nasal embryonic LHRH factor

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Nasal embryonic LHRH factor
Identifiers
Symbol(s) NELF; MGC125369; RP11-48C7.1
External IDs OMIM: 608137 MGI: 1861755 HomoloGene: 10648
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 26012 56876
Ensembl ENSG00000165802 ENSMUSG00000006476
Uniprot Q6X4W1 Q99NF2
Refseq NM_015537 (mRNA)
NP_056352 (protein)		 NM_001039386 (mRNA)
NP_001034475 (protein)
Location Chr 9: 139.46 - 139.47 Mb Chr 2: 24.88 - 24.88 Mb
Pubmed search [1] [2]

Nasal embryonic LHRH factor, also known as NELF, is a human gene.[1]


[edit] References

  1. ^ Entrez Gene: NELF nasal embryonic LHRH factor.

[edit] Further reading

  • Kramer PR, Wray S (2000). "Novel gene expressed in nasal region influences outgrowth of olfactory axons and migration of luteinizing hormone-releasing hormone (LHRH) neurons.". Genes Dev. 14 (14): 1824-34. PMID 10898796. 
  • Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.". Genome Res. 11 (3): 422-35. doi:10.1101/gr.154701. PMID 11230166. 
  • 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. 
  • 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. 
  • Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9.". Nature 429 (6990): 369-74. doi:10.1038/nature02465. PMID 15164053. 
  • Miura K, Acierno JS, Seminara SB (2004). "Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH).". J. Hum. Genet. 49 (5): 265-8. doi:10.1007/s10038-004-0137-4. PMID 15362570. 
  • 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. 
  • Nousiainen M, Silljé HH, Sauer G, et al. (2006). "Phosphoproteome analysis of the human mitotic spindle.". Proc. Natl. Acad. Sci. U.S.A. 103 (14): 5391-6. doi:10.1073/pnas.0507066103. PMID 16565220. 
  • Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.". Cell 125 (4): 801-14. doi:10.1016/j.cell.2006.03.032. PMID 16713569. 
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