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GENE - TERM ANNOTATION REPORT

CRRD ID: 1320964
Species: Mus musculus
CRRD Object: Gene
Symbol: Alx4
Name: aristaless-like homeobox 4
Acc ID: DOID:0060285
Term: parietal foramina
Definition: An inherited neural tube defect that is characterized by enlarged openings in the parietal bones of the skull, has_material_basis_in mutation in the ALX4 gene or MSX2 gene. (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/enlarged-parietal-foramina
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.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 IEA 13592920MouseDOOMIM:168500 , OMIM:609566 , OMIM:609597

 
 ISORGD:13209638554872ClinVarClinVar Annotator: match by term: Enlarged parietal foramina

 
 ISSRGD:132096313592920MouseDOOMIM:168500 , OMIM:609566 , OMIM:609597

 
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.