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Genes search result for Rattus norvegicus
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6 records found for search term Abcc6
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
620268Abcc6ATP binding cassette subfamily C member 6ENCODES a protein that exhibits ABC-type xenobiotic transporter activity; ATP binding; ATP hydrolysis activity; INVOLVED IN ATP transport; inorganic diphosphate transport; intracellular phosphate ion homeostasis; PARTICIPATES IN multidrug resistance-associated protein mediated transport pathway; ASS1105583681105637895Rat285symbol , PhenoGengene, protein-coding, PROVISIONAL [RefSeq]
10413843Abcc6em1QljuATP-binding cassette, subfamily C (CFTR/MRP), member 6; zinc finger nuclease induced mutant 1, Qiaoli LiThis allele was made by ZFN mutagenesis.ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 10-bp deletion from cDNA position 44-53 (CAGGCCTGARatsymbol , description , old_gene_symbolgene, allele
10413846Abcc6em2QljuATP-binding cassette, subfamily C (CFTR/MRP), member 6; zinc finger nuclease induced mutant 2, Qiaoli LiASSOCIATED WITH increased circulating phosphate level; ASSOCIATED WITH pseudoxanthoma elasticumRat2symbol , description , old_gene_symbolgene, allele
10413847Abcc6em3QljuATP-binding cassette, subfamily C (CFTR/MRP), member 6; zinc finger nuclease induced mutant 3, Qiaoli LiASSOCIATED WITH pseudoxanthoma elasticumRat1symbol , description , old_gene_symbolgene, allele
10413848Abcc6em4QljuATP-binding cassette, subfamily C (CFTR/MRP), member 6; zinc finger nuclease induced mutant 4, Qiaoli LiASSOCIATED WITH pseudoxanthoma elasticumRat1symbol , description , old_gene_symbolgene, allele
10413849Abcc6em5QljuATP-binding cassette, subfamily C (CFTR/MRP), member 6; zinc finger nuclease induced mutant 5, Qiaoli LiThis allele was made by ZFN mutagenesis. ZFNs were designed to target exon 1 of rat Abcc6 gene at the binding site/cutting site 5-CACGCCTGGAGAGTCCTGcgcaggCCTGAGGGTGAGTCC-3 (c.24-c.62). The resulting mutation is a 11-bp deletion from cDNA position 39-49 (CTGCGCAGRatsymbol , description , old_gene_symbolgene, allele