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48 records found for search term Dnajc11
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
12896005CV390521duplicationNM_018198.4(DNAJC11):c.1098-32dupnot specified [RCV000454752]benign166400716640072Humanname
329371954CV2455007single nucleotide variantNM_018198.4(DNAJC11):c.28C>G (p.Leu10Val)not specified [RCV004272269]uncertain significance167017736701773Humanname
155917617CV2274951single nucleotide variantNM_018198.4(DNAJC11):c.164C>T (p.Ala55Val)not specified [RCV004135003]uncertain significance166809466680946Humanname
156352190CV2323921single nucleotide variantNM_018198.4(DNAJC11):c.221C>A (p.Thr74Asn)not specified [RCV004176447]uncertain significance166784496678449Humanname
598163375CV3953482single nucleotide variantNM_018198.4(DNAJC11):c.213C>G (p.Asp71Glu)not specified [RCV005329349]uncertain significance166784576678457Humanname
598163380CV3953483single nucleotide variantNM_018198.4(DNAJC11):c.277G>A (p.Val93Ile)not specified [RCV005329350]uncertain significance166678106667810Humanname
15191613CV696850single nucleotide variantNM_018198.4(DNAJC11):c.1497G>A (p.Ser499=)not provided [RCV000954828]benign166372256637225Humanname
15181786CV719057single nucleotide variantNM_018198.4(DNAJC11):c.1599C>T (p.Gly533=)not provided [RCV000885843]benign166361726636172Humanname
155983519CV2241018single nucleotide variantNM_018198.4(DNAJC11):c.916G>A (p.Ala306Thr)not specified [RCV004104071]uncertain significance166451056645105Humanname
156136443CV2284816single nucleotide variantNM_018198.4(DNAJC11):c.593C>T (p.Ala198Val)not specified [RCV004142992]uncertain significance166528666652866Humanname
155909626CV2303425single nucleotide variantNM_018198.4(DNAJC11):c.931C>G (p.Gln311Glu)not specified [RCV004159763]uncertain significance166450906645090Humanname
155924033CV2347610single nucleotide variantNM_018198.4(DNAJC11):c.686G>A (p.Arg229His)not specified [RCV004200548]uncertain significance166515476651547Humanname
155939190CV2376590single nucleotide variantNM_018198.4(DNAJC11):c.425A>G (p.Tyr142Cys)not specified [RCV004220751]uncertain significance166539936653993Humanname
329397994CV2466515single nucleotide variantNM_018198.4(DNAJC11):c.924C>G (p.Ile308Met)not specified [RCV004274058]uncertain significance166450976645097Humanname
401724562CV2677919single nucleotide variantNM_018198.4(DNAJC11):c.713C>T (p.Thr238Ile)not specified [RCV004294406]uncertain significance166459706645970Humanname
401740729CV2702604single nucleotide variantNM_018198.4(DNAJC11):c.823G>A (p.Gly275Ser)not specified [RCV004317086]uncertain significance166458606645860Humanname
405732059CV3240713single nucleotide variantNM_018198.4(DNAJC11):c.554C>T (p.Ser185Leu)not specified [RCV004379333]uncertain significance166529056652905Humanname
405732065CV3240714single nucleotide variantNM_018198.4(DNAJC11):c.757G>A (p.Gly253Ser)not specified [RCV004379334]uncertain significance166459266645926Humanname
597643862CV3662941single nucleotide variantNM_018198.4(DNAJC11):c.591T>G (p.Phe197Leu)not specified [RCV004909555]uncertain significance166528686652868Humanname
598163386CV3953484single nucleotide variantNM_018198.4(DNAJC11):c.742C>T (p.Arg248Cys)not specified [RCV005329351]uncertain significance166459416645941Humanname
8625042CV80161single nucleotide variantNM_018198.3(DNAJC11):c.712A>T (p.Thr238Ser)Malignant melanoma [RCV000060237]not provided166459716645971Humanname
8629640CV84787single nucleotide variantNM_018198.3(DNAJC11):c.310C>T (p.Arg104Ter)Malignant melanoma [RCV000064869]not provided166677776667777Humanname
156181712CV2246305single nucleotide variantNM_018198.4(DNAJC11):c.1604T>C (p.Leu535Pro)not specified [RCV004107751]uncertain significance166361676636167Humanname
156161611CV2246424single nucleotide variantNM_018198.4(DNAJC11):c.1303A>C (p.Lys435Gln)not specified [RCV004110196]uncertain significance166383156638315Humanname
156198485CV2334568single nucleotide variantNM_018198.4(DNAJC11):c.1081G>A (p.Val361Ile)not specified [RCV004181668]uncertain significance166445746644574Humanname
155970428CV2338062single nucleotide variantNM_018198.4(DNAJC11):c.1358T>C (p.Ile453Thr)not specified [RCV004186101]uncertain significance166374706637470Humanname
155913873CV2341876single nucleotide variantNM_018198.4(DNAJC11):c.1661G>A (p.Arg554Lys)not specified [RCV004184825]uncertain significance166356946635694Humanname
156341816CV2344969single nucleotide variantNM_018198.4(DNAJC11):c.1600G>A (p.Val534Ile)not specified [RCV004193263]uncertain significance166361716636171Humanname
401737494CV2699831single nucleotide variantNM_018198.4(DNAJC11):c.1025A>C (p.Lys342Thr)not specified [RCV004308476]uncertain significance166446306644630Humanname
401752476CV2707022single nucleotide variantNM_018198.4(DNAJC11):c.1207A>G (p.Met403Val)not specified [RCV004321618]uncertain significance166399486639948Humanname
401762536CV2714180single nucleotide variantNM_018198.4(DNAJC11):c.1033A>G (p.Arg345Gly)not specified [RCV004317420]uncertain significance166446226644622Humanname
401781390CV2730487single nucleotide variantNM_018198.4(DNAJC11):c.1321G>A (p.Ala441Thr)not specified [RCV004331525]uncertain significance166382976638297Humanname
401769761CV2731611single nucleotide variantNM_018198.4(DNAJC11):c.1282G>A (p.Ala428Thr)not specified [RCV004330954]uncertain significance166383366638336Humanname
401897596CV2776406single nucleotide variantNM_018198.4(DNAJC11):c.1042G>A (p.Val348Ile)not specified [RCV004355532]uncertain significance166446136644613Humanname
405731999CV3240705single nucleotide variantNM_018198.4(DNAJC11):c.1064T>C (p.Val355Ala)not specified [RCV004379325]uncertain significance166445916644591Humanname
405732005CV3240706single nucleotide variantNM_018198.4(DNAJC11):c.1180G>A (p.Val394Met)not specified [RCV004379326]uncertain significance166399756639975Humanname
405732012CV3240707single nucleotide variantNM_018198.4(DNAJC11):c.1208T>G (p.Met403Arg)not specified [RCV004379327]uncertain significance166399476639947Humanname
405732023CV3240708single nucleotide variantNM_018198.4(DNAJC11):c.1214G>A (p.Arg405His)not specified [RCV004379328]uncertain significance166399416639941Humanname
405732030CV3240709single nucleotide variantNM_018198.4(DNAJC11):c.1511C>T (p.Thr504Met)not specified [RCV004379329]uncertain significance166372116637211Humanname
405732038CV3240710single nucleotide variantNM_018198.4(DNAJC11):c.1564G>A (p.Glu522Lys)not specified [RCV004379330]uncertain significance166362076636207Humanname
405732045CV3240711single nucleotide variantNM_018198.4(DNAJC11):c.1676G>A (p.Gly559Glu)not specified [RCV004379331]uncertain significance166356796635679Humanname
407497338CV3437513single nucleotide variantNM_018198.4(DNAJC11):c.1582C>G (p.Leu528Val)not specified [RCV004622175]uncertain significance166361896636189Humanname
597643840CV3662937single nucleotide variantNM_018198.4(DNAJC11):c.1252A>C (p.Lys418Gln)not specified [RCV004909552]uncertain significance166399036639903Humanname
597643847CV3662938single nucleotide variantNM_018198.4(DNAJC11):c.1299G>T (p.Gln433His)not specified [RCV004909553]uncertain significance166383196638319Humanname
597643855CV3662939single nucleotide variantNM_018198.4(DNAJC11):c.1393G>A (p.Val465Ile)not specified [RCV004909554]uncertain significance166373296637329Humanname
598163369CV3953481single nucleotide variantNM_018198.4(DNAJC11):c.1358T>A (p.Ile453Asn)not specified [RCV005329348]uncertain significance166374706637470Humanname
598163393CV3953485single nucleotide variantNM_018198.4(DNAJC11):c.1603C>G (p.Leu535Val)not specified [RCV005329352]uncertain significance166361686636168Humanname
598163399CV3953486single nucleotide variantNM_018198.4(DNAJC11):c.1393G>C (p.Val465Leu)not specified [RCV005329353]uncertain significance166373296637329Humanname