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GENE - TERM ANNOTATION REPORT

RGD ID: 8831957
Species: Chinchilla lanigera
RGD Object: Gene
Symbol: Lama5
Name: laminin subunit alpha 5
Acc ID: DOID:4621
Term: holoprosencephaly
Definition: A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Holoprosencephaly "DO" "DO", http://www.ncbi.nlm.nih.gov/books/NBK1530/ "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)
Lama5 ISOLAMA5 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Holoprosencephaly sequencePMID:25741868 PMID:28492532 PMID:28735299 PMID:29534211 PMID:31680349
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