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GENE - TERM ANNOTATION REPORT

RGD ID: 11825349
Species: Pan paniscus
RGD Object: Gene
Symbol: MYO5B
Name: myosin VB
Acc ID: DOID:0060775
Term: microvillus inclusion disease
Definition: A congenital diarrhea characterized by onset of intractable life-threatening watery diarrhea during infancy, lack of microvilli on the surface of enterocytes and occurrence of intracellular vacuolar structures containing microvilli that has_material_basis_in homozygous or compound heterozygous mutation in the MYO5B gene on chromosome 18q21. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/18724368 "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)
MYO5B ISOMYO5B (Homo sapiens)7240710OMIM  
MYO5B ISOMYO5B (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital microvillous atrophy | ClinVar Annotator: match by term: Diarrhea with Microvillus Atrophy | ClinVar Annotator: match by term: MYO5B-related conditionPMID:16199547 PMID:17576681 PMID:18724368 PMID:19006234 PMID:20186687 PMID:21206382 PMID:21282656 PMID:24014347 PMID:24033266 PMID:25111220 PMID:25741868 PMID:26553929 PMID:27242896 PMID:27532546 PMID:28027573 PMID:28492532 PMID:28899465 PMID:29218485 PMID:29266534 PMID:31750554 PMID:32304554 PMID:32888943 PMID:33525641 PMID:9536098
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