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GENE - TERM ANNOTATION REPORT

RGD ID: 12346305
Species: Canis lupus familiaris
RGD Object: Gene
Symbol: SLC33A1
Name: solute carrier family 33 member 1
Acc ID: DOID:9005895
Term: Congenital Cataracts, Hearing Loss, and Neurodegeneration
Definition: null
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)
SLC33A1 ISOSLC33A1 (Homo sapiens)7240710OMIM  
SLC33A1 ISOSLC33A1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Huppke-Brendel syndrome | ClinVar Annotator: match by term: SLC33A1-related conditionPMID:15902551 PMID:22243965 PMID:22508683 PMID:24215330 PMID:25741868 PMID:26467025 PMID:27306358 PMID:28492532 PMID:29908077 PMID:31194315 PMID:35999711
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