Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

RGD ID: 1563910
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Lmbr1
Name: limb development membrane protein 1
Acc ID: DOID:9002066
Term: Developmental Delay with Hypotonia, Myopathy, and Brain Abnormalities
Definition: An autosomal recessive disorder characterized by global developmental delay and muscle weakness apparent in infancy. Caused by homozygous mutation in the GOLGA2 gene on chromosome 9q34.
Definition Source(s): OMIM:620240
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)
Go Back to source page   Continue to Ontology report