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GENE - TERM ANNOTATION REPORT

RGD ID: 18920641
Species: Heterocephalus glaber
RGD Object: Gene
Symbol: Trappc14
Name: trafficking protein particle complex subunit 14
Acc ID: DOID:9003084
Term: Primary Autosomal Recessive Microcephaly 25
Definition: MCPH25 is caused by homozygous mutation in the MAP11 gene on chromosome 7q22. (OMIM)
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)
Trappc14 ISOTRAPPC14 (Homo sapiens)7240710OMIM  
Trappc14 ISOTRAPPC14 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Microcephaly 25, primary, autosomal recessivePMID:25741868 PMID:30715179
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