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VARIANT - TERM ANNOTATION REPORT

RGD ID: 8557835
Species: Homo sapiens
RGD Object: Variant
Symbol: CV19031
Name: NM_017739.3(POMGNT1):c.1324C>T (p.Arg442Cys)
Acc ID: DOID:0110292
Term: autosomal recessive limb-girdle muscular dystrophy type 2O
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding protein O-mannose beta-1,2-N-acetylglucosaminyltransferase (POMGNT1) on chromosome 1p34. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/18195152 "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)
CV19031 IAGP 8554872ClinVarClinVar Annotator: match by term: Limb-girdle muscular dystrophy-dystroglycanopathy type C3

PMID:15236414 PMID:16427280 PMID:17906881 PMID:21361872 PMID:25390965 PMID:25741868 PMID:26467025 PMID:28492532
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