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FLASH GENE
Symbol DMRT3 contributors: mct/npt - updated : 30-03-2018
HGNC name doublesex and mab-3 related transcription factor 3
HGNC id 13909
ASSOCIATED DISORDERS
corresponding disease(s)
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional   deletion    
of the cis-regulatory element for DMRT3 in humans may cause impaired development of the forebrain and gait abnormalities, resulting in spastic Cerebral palsy (CP)
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS