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GENE - TERM ANNOTATION REPORT

RGD ID: 18536351
Species: Chlorocebus sabaeus
RGD Object: Gene
Symbol: SLC25A19
Name: solute carrier family 25 member 19
Acc ID: DOID:10907
Term: microcephaly
Definition: A congenital nervous system abnormality that is characterized by a significantly smaller than normal head in infants. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Microcephaly "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)
SLC25A19 ISOSLC25A19 (Homo sapiens)9068941RGDMicrocephaly, Amish type, OMIM:607196;DNA:point mutation:exon:G177APMID:12185364 REF_RGD_ID:1624242
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