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GENE - TERM ANNOTATION REPORT

RGD ID: 1603695
Species: Homo sapiens
RGD Object: Gene
Symbol: RPGRIP1L
Name: RPGRIP1 like
Acc ID: DOID:2975
Term: cystic kidney disease
Definition: A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC).
Definition Source(s): MESH:D052177
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)
RPGRIP1L IAGP 11073359RGDassociated with Meckel Syndrome, Type 5;DNA:mutations:exons: 
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