ANKRD11 FISH Probe

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 Details
SKU Test Kits Buffer Dye Color Order Now
ANKRD11-20-RE 20 (40 μL) 200 μL color Request Pricing
ANKRD11-20-OR 20 (40 μL) 200 μL color Request Pricing
ANKRD11-20-GO 20 (40 μL) 200 μL color Request Pricing
ANKRD11-20-GR 20 (40 μL) 200 μL color Request Pricing
ANKRD11-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

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 Details

Gene Symbol : ANKRD11

Gene Name : Ankyrin repeat domain 11

Chromosome : CHR 16: 894,905,60-892,676,18

Locus : 16q24.3

Alt. Genes : KIF20A

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