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FLASH GENE
Symbol VSX2 contributors: mct - updated : 26-04-2017
HGNC name visual system homeobox 2
HGNC id 1975
ASSOCIATED DISORDERS
corresponding disease(s) MCIA , MCOP2
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional germinal mutation      
cause reduced proliferation of retinal progenitor cells during development, leading to microphthalmia
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS