Gene: ANKRD11

Alternate names for this Gene: ANCO-1|ANCO1|LZ16|T13

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.

Gene is located in Chromosome: 16

Location in Chromosome : 16q24.3

Description of this Gene: ankyrin repeat domain 11

Type of Gene: protein-coding

Gene: LOC105371414

Alternate names for this Gene: -

Gene Summary:

Gene is located in Chromosome: 16

Location in Chromosome : 16q24.3

Description of this Gene: uncharacterized LOC105371414

Type of Gene: ncRNA