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This locus encodes an ankryin repeat domain-containing protein. Additionally we are shipping ANKRD11 Antibodies (25) and many more products for this protein.
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Further delineation of the KBG syndrome phenotype on large patients cohort caused by ANKRD11 aberrations has been presented.
we conclude that severe short stature, intellectual disability, and macrodontia are the main characteristics in KBG syndrome related to ANKRD11 mutation
ANKRD11 C-terminus plays an important role in regulating the abundance of the protein, and a disturbance of the protein abundance due to the mutations leads to KBG syndrome.
AIB1 (show NCOA3 ELISA Kits), AIB1 (show NCOA3 ELISA Kits)-delta4 and ANCO1 (show ANKRD12 ELISA Kits) are important determinants of endocrine and growth factor responsiveness in breast cancer.
The complete neurological and psychiatric features observed in two patients with KBG syndrome due to ANKRD11 mutations, are reported.
Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndrome.
aberrant DNA methylation (show HELLS ELISA Kits) of three CpGs in a 19 bp region within the ANKRD11 promoter may be responsible for its down-regulation in breast cancer.
Mutations in ANKRD11 cause KBG syndrome and outline a fundamental role of ANKRD11 in craniofacial, dental, skeletal, and central nervous system development and function.
ANKRD11 is a candidate gene for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.
Together, these results indicate that the transcriptional potential of ANCO-1 (show ANKRD12 ELISA Kits) may be modulated by a combination of repression and activation signals.
A Glu (show GCG ELISA Kits)->Lys (show LYZ ELISA Kits) missense mutation in a highly conserved region causes osteopenia and craniofacial abnormalities. Homozygosity causes embryo death. Ankrd11 is a genetic regular of bone homeostasis.
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.
ankyrin repeat domain 11
, ankyrin repeat domain-containing protein 11-like
, ankyrin repeat domain-containing protein 11
, ankyrin repeat-containing cofactor 1
, nasopharyngeal carcinoma susceptibility protein