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GENE - TERM ANNOTATION REPORT

RGD ID: 1563513
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Slc10a3
Name: solute carrier family 10, member 3
Acc ID: DOID:607
Term: paraplegia
Definition: Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness.
Definition Source(s): MESH:D010264
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.
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