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15 records found for search term Spata7
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
621010Spata7spermatogenesis associated 7INVOLVED IN spermatogenesis; microtubule cytoskeleton organization (ortholog); photoreceptor cell maintenance (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN axoneme (ortholog); ciliary basal body (ortholog); ciliar6123609519123655001Rat126symbol , PhenoGengene, protein-coding, VALIDATED [RefSeq]
1345087SPATA7spermatogenesis associated 7This gene, originally isolated from testis, is also expressed in retina. Mutations in this gene are associated with Leber congenital amaurosis and juvenile retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, 148838565788470350Human351symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1617430Spata7spermatogenesis associated 7Involved in microtubule cytoskeleton organization; photoreceptor cell maintenance; and protein localization to non-motile cilium. Located in photoreceptor distal connecting cilium. Is active in rod photoreceptor outer segment. Is expressed in several structures, including blood vessel; central nervo129859416998636078Mouse131symbol , PhenoGen , descriptiongene, protein-coding, VALIDATED [RefSeq]
9031659Spata7spermatogenesis associated 7INVOLVED IN microtubule cytoskeleton organization (ortholog); photoreceptor cell maintenance (ortholog); protein localization to photoreceptor connecting cilium (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN axonemNW_0049554381103308911069178Chinchilla30symbolgene, protein-coding, MODEL [RefSeq]
11786968SPATA7spermatogenesis associated 7INVOLVED IN spermatogenesis (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN photoreceptor distal connecting cilium (ortholog)146900272369056185Bonobo33symbolgene, protein-coding, MODEL [RefSeq]
12079909SPATA7spermatogenesis associated 7INVOLVED IN spermatogenesis (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN axoneme (inferred); ciliary basal body (inferred); ciliary transition zone (inferred)85965829559697409Dog32symbolgene, protein-coding, MODEL [RefSeq]
12701768Spata7spermatogenesis associated 7INVOLVED IN spermatogenesis (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN photoreceptor distal connecting cilium (ortholog)NW_0049364881587816715911301Squirrel33symbolgene, protein-coding, MODEL [RefSeq]
18661906SPATA7spermatogenesis associated 7INVOLVED IN spermatogenesis (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN photoreceptor distal connecting cilium (ortholog)Green Monkey33symbolgene, protein-coding, MODEL [RefSeq]
18927281Spata7spermatogenesis associated 7INVOLVED IN protein localization to photoreceptor connecting cilium (ortholog); protein localization to photoreceptor outer segment (ortholog); spermatogenesis (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN ciliaryNaked Mole-Rat30symbolgene, protein-coding, MODEL [RefSeq]
626001992Spata7spermatogenesis associated 7INVOLVED IN microtubule cytoskeleton organization (ortholog); photoreceptor cell maintenance (ortholog); protein localization to photoreceptor connecting cilium (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN axonemBlack Rat27symbolgene, protein-coding, MODEL [RefSeq]
14120323SPATA7spermatogenesis associated 7INVOLVED IN spermatogenesis (ortholog); ASSOCIATED WITH fundus dystrophy (ortholog); genetic disease (ortholog); Leber congenital amaurosis (ortholog); FOUND IN axoneme (inferred); ciliary basal body (inferred); ciliary transition zone (inferred)Pig32symbolgene, protein-coding, PROVISIONAL [RefSeq]
284142973spata7Tropical Clawed Frogsymbolgene, null
284142209spata7.LAfrican Clawed Frogsymbolgene, null
16555948AC073587.1spermatogenesis associated 7 (SPATA7) pseudogeneHumannamegene, unprocessed_pseudogene
1557648Clec2mC-type lectin domain family 2, member mENCODES a protein that exhibits carbohydrate binding (inferred); FOUND IN membrane (inferred); INTERACTS WITH Butylbenzyl phthalate; sodium arsenite; bisphenol A (ortholog)6129299128129308770Mouse10old_gene_symbolgene, protein-coding, VALIDATED [RefSeq]