| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ANKRD11-C16orf7-20-RERE | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-REOR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-REGO | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-REGR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-REAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-ORRE | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-OROR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-ORGO | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-ORGR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-ORAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GORE | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GOOR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GOGO | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GOGR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GOAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GRRE | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GROR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GRGO | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GRGR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-GRAQ | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-AQRE | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-AQOR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-AQGO | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-AQGR | 20 (40 μL) | 200 μL |
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| ANKRD11-C16orf7-20-AQAQ | 20 (40 μL) | 200 μL |
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This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay, seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 2 and X. [provided by RefSeq, Jan 2012]
Gene Symbol : ANKRD11
Gene Name : Ankyrin repeat domain 11
Chromosome : CHR 16: 894,905,60-892,676,18
Locus : 16q24.3
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