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GENE - TERM ANNOTATION REPORT

RGD ID: 732353
Species: Mus musculus
RGD Object: Gene
Symbol: Slc24a1
Name: solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
Acc ID: DOID:0110867
Term: congenital stationary night blindness 1C
Definition: A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/19878917 "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)
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