An integrated knowledge database dedicated to ncRNAs, especially lncRNAs.
NONCODE and Disease

Search Type: *Only support human


This search panel allows you to search information about mutation and disease relation about long non-coding RNA. You can enter NONCODE ID or mutation name or disease name. more ...


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*Only support human

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NONCODE IDGene SymbolDisease nameSource DatabaseSource PMID
NONHSAG016288.2C15orf2Angelman syndromeLncRNADisease17337158
NONHSAG016288.2C15orf2Prader-Willi syndromeLncRNADisease17337158
NONHSAG016292.2C15orf2Angelman syndromeLncRNADisease17337158
NONHSAG016292.2C15orf2Prader-Willi syndromeLncRNADisease17337158
NONHSAG016292.2PWRN1Prader-Willi syndromeLncRNAWiki0
NONHSAG016293.2C15orf2Angelman syndromeLncRNADisease17337158
NONHSAG016293.2C15orf2Prader-Willi syndromeLncRNADisease17337158
NONHSAG016295.2C15orf2Angelman syndromeLncRNADisease17337158
NONHSAG016295.2C15orf2Prader-Willi syndromeLncRNADisease17337158
NONHSAG016298.2C15orf2Angelman syndromeLncRNADisease17337158
NONHSAG016298.2C15orf2Prader-Willi syndromeLncRNADisease17337158
NONHSAG016307.3IPWPrader-Willi syndromeLncRNADisease24816254
NONHSAG016307.3IPWPrader-Willi syndromeMNDR9063754
NONHSAG016307.3IPWPrader-Willi syndromeLncRNADisease23791884
NONHSAG016307.3IPWPrader-Willi syndromeLncRNADisease7849716