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GENE - TERM ANNOTATION REPORT

RGD ID: 1602004
Species: Homo sapiens
RGD Object: Gene
Symbol: B9D1
Name: B9 domain containing 1
Acc ID: DOID:9001634
Term: Meckel Syndrome 9
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)
B9D1 IAGP 7240710OMIM  
B9D1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel syndrome, type 9PMID:21493627 PMID:25741868 PMID:28492532
B9D1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel syndrome, type 9PMID:25741868 PMID:28492532
B9D1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel syndrome, type 9PMID:25741868
B9D1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel syndrome, type 9PMID:25741913
B9D1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel syndrome, type 9 
B9D1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel syndrome, type 9PMID:28492532
B9D1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Meckel syndrome, type 9PMID:21493627
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