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GENE - TERM ANNOTATION REPORT

RGD ID: 1342524
Species: Homo sapiens
RGD Object: Gene
Symbol: STK25
Name: serine/threonine kinase 25
Acc ID: DOID:0110781
Term: hereditary spastic paraplegia 30
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the KIF1A gene on chromosome 2q37. (DO)
Definition Source(s): https://pubmed.ncbi.nlm.nih.gov/31488895/ "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/21487076 "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)
STK25 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hereditary spastic paraplegia 30PMID:28492532
STK25 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hereditary spastic paraplegia 30PMID:16081310 PMID:20020533 PMID:20691407 PMID:21384162 PMID:21820098 PMID:24715439 PMID:28492532 PMID:30848064 PMID:31488895
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