OVOL2 FISH Probe

This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy. [provided by RefSeq, Apr 2016]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
OVOL2-20-RE 20 (40 μL) 200 μL color Request Pricing
OVOL2-20-OR 20 (40 μL) 200 μL color Request Pricing
OVOL2-20-GO 20 (40 μL) 200 μL color Request Pricing
OVOL2-20-GR 20 (40 μL) 200 μL color Request Pricing
OVOL2-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy. [provided by RefSeq, Apr 2016]

Gene Details

Gene Symbol : OVOL2

Gene Name : Ovo like zinc finger 2

Chromosome : CHR 20: 180,591,87-180,241,51

Locus : 20p11.23

Alt. Genes : RBM12

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