ANKRD11

gene product
LZ16, T13
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]
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125 antibodies from 20 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
OriGene
2 antibodies
Novus Biologicals
5 antibodies
antibodies-online
43 antibodies
LifeSpan BioSciences, Inc.
12 antibodies
Aviva Systems Biology
1 antibody
Invitrogen Antibodies
3 antibodies
GeneTex
1 antibody
Biorbyt
14 antibodies
NovoPro Bioscience Inc.
1 antibody
Proteintech Group
1 antibody
Atlas Antibodies
2 antibodies
Creative Biolabs
4 antibodies
Abnova Corporation
1 antibody
Creative Diagnostics
2 antibodies
MyBioSource
2 antibodies
Abbexa
3 antibodies
GenWay
2 antibodies
Sigma-Aldrich
1 antibody
United States Biological
1 antibody