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RGD ID: 1642882
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Rab1b
Name: RAB1B, member RAS oncogene family
Acc ID: DOID:0070133
Term: autosomal recessive cutis laxa type IB
Definition: An autosomal recessive cutis laxa type I characterized by disturbed elastic fiber formation resulting in severe systemic connective tissue abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the EFEMP2 gene on chromosome 11q13. (DO)
Definition Source(s): "DO" "DO", "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)
Rab1b ISORAB1B (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Cutis laxa, autosomal recessive, type 1BPMID:28492532
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