EML1

Echinoderm microtubule associated protein like 1, also known as EML1, is a human gene.cite web | title = Entrez Gene: EML1 echinoderm microtubule associated protein like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2009| accessdate = ]

PBB_Summary
section_title =
summary_text = Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene.cite web | title = Entrez Gene: EML1 echinoderm microtubule associated protein like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2009| accessdate = ]

References

Further reading

PBB_Further_reading
citations =
*cite journal | author=Kaplan J, Gerber S, Bonneau D, "et al." |title=A gene for Usher syndrome type I (USH1A) maps to chromosome 14q. |journal=Genomics |volume=14 |issue= 4 |pages= 979–87 |year= 1993 |pmid= 1478676 |doi=
*cite journal | author=Andersson B, Wentland MA, Ricafrente JY, "et al." |title=A "double adaptor" method for improved shotgun library construction. |journal=Anal. Biochem. |volume=236 |issue= 1 |pages= 107–13 |year= 1996 |pmid= 8619474 |doi= 10.1006/abio.1996.0138
*cite journal | author=Yu W, Andersson B, Worley KC, "et al." |title=Large-scale concatenation cDNA sequencing. |journal=Genome Res. |volume=7 |issue= 4 |pages= 353–8 |year= 1997 |pmid= 9110174 |doi=
*cite journal | author=Eudy JD, Ma-Edmonds M, Yao SF, "et al." |title=Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32. |journal=Genomics |volume=43 |issue= 1 |pages= 104–6 |year= 1997 |pmid= 9226380 |doi=
*cite journal | author=Schaefer GB, Bodensteiner JB, Thompson JN, "et al." |title=Volumetric neuroimaging in Usher syndrome: evidence of global involvement. |journal=Am. J. Med. Genet. |volume=79 |issue= 1 |pages= 1–4 |year= 1999 |pmid= 9738858 |doi=
*cite journal | author=Lepley DM, Palange JM, Suprenant KA |title=Sequence and expression patterns of a human EMAP-related protein-2 (HuEMAP-2). |journal=Gene |volume=237 |issue= 2 |pages= 343–9 |year= 1999 |pmid= 10521658 |doi=
*cite journal | author=Ly CD, Roche KW, Lee HK, Wenthold RJ |title=Identification of rat EMAP, a delta-glutamate receptor binding protein. |journal=Biochem. Biophys. Res. Commun. |volume=291 |issue= 1 |pages= 85–90 |year= 2002 |pmid= 11829466 |doi= 10.1006/bbrc.2002.6413
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Rual JF, Venkatesan K, Hao T, "et al." |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209

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