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GENE - TERM ANNOTATION REPORT

RGD ID: 1343083
Species: Homo sapiens
RGD Object: Gene
Symbol: NONO
Name: non-POU domain containing octamer binding
Acc ID: HP:0000478
Term: Abnormality of the eye
Definition: Any abnormality of the eye, including location, spacing, and intraocular abnormalities.
Definition Source(s): https://orcid.org/0000-0002-0736-9199
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
NONO IAGP 11058183RGDDNA:nonsense mutation, silent mutation, frameshift mutation:CDS:p.R365*, p.A377A, p.N466Kfs*13 
NONO IAGP 155882460RGDDNA:SNPs:nonsense mutations, splice-site mutation:CDS, intron:c.457C>T, c.550C>T, c.1171+1G>A 
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