HMX2 FISH Probe

The protein encoded by this gene is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing this gene have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. [provided by RefSeq, Aug 2012]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
HMX2-20-RE 20 (40 μL) 200 μL color Request Pricing
HMX2-20-OR 20 (40 μL) 200 μL color Request Pricing
HMX2-20-GO 20 (40 μL) 200 μL color Request Pricing
HMX2-20-GR 20 (40 μL) 200 μL color Request Pricing
HMX2-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

The protein encoded by this gene is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing this gene have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. [provided by RefSeq, Aug 2012]

Gene Details

Gene Symbol : HMX2

Gene Name : H6 family homeobox 2

Chromosome : CHR 10: 123,142,420-123,150,672

Locus : 10q26.13

Alt. Genes : PREB

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