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GENE - TERM ANNOTATION REPORT

RGD ID: 1598543
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Cdsn
Name: corneodesmosin
Acc ID: DOID:0110699
Term: hypotrichosis 2
Definition: A hypotrichosis that has_material_basis_in a autosomal dominant mutation of the CDSN gene on chromosome 6p21.33. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/12754508 "DO" "DO"
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)
Cdsn ISOCDSN (Homo sapiens)7240710OMIM  
Cdsn ISOCDSN (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hypotrichosis 2PMID:10793007 PMID:12754508 PMID:25741868 PMID:28492532 PMID:3652491
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