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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HMX2BA-20-REGO | 20 (40 μL) | 200 μL |
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| HMX2BA-20-REGR | 20 (40 μL) | 200 μL |
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| HMX2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| HMX2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| HMX2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| HMX2BA-20-GROR | 20 (40 μL) | 200 μL |
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| HMX2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| HMX2BA-20-AQOR | 20 (40 μL) | 200 μL |
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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 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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