This gene encodes a transcription factor that belongs to the H6 family of homeobox proteins. This protein can bind a 5'-CAAG-3' core DNA sequence, and it is involved in the development of craniofacial structures. Mutations in this gene cause oculoauricular syndrome, a disorder of the eye and external ear. [provided by RefSeq, Oct 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HMX1BA-20-REGO | 20 (40 μL) | 200 μL |
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| HMX1BA-20-REGR | 20 (40 μL) | 200 μL |
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| HMX1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| HMX1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| HMX1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| HMX1BA-20-GROR | 20 (40 μL) | 200 μL |
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| HMX1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| HMX1BA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a transcription factor that belongs to the H6 family of homeobox proteins. This protein can bind a 5'-CAAG-3' core DNA sequence, and it is involved in the development of craniofacial structures. Mutations in this gene cause oculoauricular syndrome, a disorder of the eye and external ear. [provided by RefSeq, Oct 2009]
Gene Symbol : HMX1
Gene Name : H6 family homeobox 1
Chromosome : CHR 4: 887,181,6-884,607,5
Locus : 4p16.1
Alt. Genes : RBM5
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