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GENE - TERM ANNOTATION REPORT

RGD ID: 1306705
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Tmem237
Name: transmembrane protein 237
Acc ID: DOID:0050778
Term: Meckel syndrome
Definition: A ciliopathy that is characterized by renal cystic dysplasia, occipital encephalocele, polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Meckel_syndrome "DO" "DO", http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/661/viewAbstract "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)
Tmem237 ISOTMEM237 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel-Gruber syndromePMID:25558065 PMID:25741868
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