Tissue expression
Cell line expression
Protein structure

AHI1

Abelson helper integration site 1
FLJ20069, JBTS3, ORF1 
This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]
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215 antibodies from 30 providers.

Antibody properties

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AntibodyRefsTypeWBELICCIPIHCFC
Invitrogen Antibodies
13 antibodies
Proteintech Group
1 antibody
antibodies-online
58 antibodies
Novus Biologicals
10 antibodies
GeneTex
4 antibodies
Biorbyt
25 antibodies
Cusabio Biotech Co., Ltd
5 antibodies
OriGene
4 antibodies
Abnova Corporation
6 antibodies
St John's Laboratory
2 antibodies
Bethyl Laboratories
2 antibodies
Everest Biotech
1 antibody
NovoPro Bioscience Inc.
1 antibody
Wuhan Fine Biotech Co., Ltd.
1 antibody
Aviva Systems Biology
3 antibodies
Atlas Antibodies
2 antibodies
MilliporeSigma / Merck KGaA
4 antibodies
Acris Antibodies GmbH
1 antibody
Affinity Biosciences
1 antibody
Creative Diagnostics
1 antibody
Signalway Antibody LLC
1 antibody
Leading Biology
3 antibodies
Abgent
2 antibodies
Abbexa
1 antibody
MyBioSource
3 antibodies
United States Biological
13 antibodies
Creative Biolabs
2 antibodies
ProSci
1 antibody