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EML1


Official Full Name
EMAP like 1
Organism
Homo sapiens
Gene ID
2009
Background
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. [provided by RefSeq, Jul 2008]
Synonyms
BH; EMAP; ELP79; EMAPL; EMAP-1

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MiUTR1R-01720 EML1 miRNA 3'UTR clone Inquiry
MiUTR1M-04381 EML1 miRNA 3'UTR clone Inquiry
MiUTR1H-03213 EML1 miRNA 3'UTR clone Inquiry
MiUTR1H-03212 EML1 miRNA 3'UTR clone Inquiry
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CDCR371070 Rat Eml1 ORF Clone(NM_001025741.1) Inquiry
CDCR060148 Mouse Eml1 ORF clone (NM_001043336.1) Inquiry
CDCR060146 Mouse Eml1 ORF clone (NM_001043335.1) Inquiry
CDCR060142 Human EML1 ORF clone (NM_004434.2) Inquiry
CDCR060140 Human EML1 ORF clone (NM_001008707.1) Inquiry
CDCB186108 Rabbit EML1 ORF clone (XM_008251900.1) Inquiry
CDCS406382 Human EML1 ORF Clone (BC032541) Inquiry
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