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Genes search result for Homo sapiens
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2 records found for search term Abhd11
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1606493ABHD11abhydrolase domain containing 11This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Mar 2016]77373609473738802Human97symbol , old_gene_name , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1342590BICDL3PBICD family like 3, pseudogeneINTERACTS WITH cadmium dichloride; cisplatin; propofol77373506973736000Human12old_gene_name , old_gene_symbolgene, pseudo, VALIDATED [RefSeq]