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FLASH GENE
Symbol DMRT2 contributors: np/mct - updated : 29-03-2020
HGNC name doublesex and mab-3 related transcription factor 2
HGNC id 2935
ASSOCIATED DISORDERS
corresponding disease(s) SRA2
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation      
mutations in DMRT2 are likely associated with a different (novel) subtype of SCD mainly characterized by severe rib anomalies but lacking clear segmentation defects of the vertebral bodies
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS
  • Dmrt2 knock-out mice exhibit severe rib and vertebral defects