EVC2

gene product
LBN
This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
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121 antibodies from 26 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
Novus Biologicals
4 antibodies
antibodies-online
37 antibodies
LifeSpan BioSciences, Inc.
8 antibodies
OriGene
4 antibodies
Biorbyt
11 antibodies
Invitrogen Antibodies
4 antibodies
GeneTex
3 antibodies
Atlas Antibodies
2 antibodies
Aviva Systems Biology
2 antibodies
Abnova Corporation
1 antibody
Signalway Antibody LLC
1 antibody
Antibodies.com
1 antibody
Acris Antibodies GmbH
2 antibodies
Everest Biotech
1 antibody
NSJ Bioreagents
1 antibody
Abgent
2 antibodies
Arigo
1 antibody
Creative Biolabs
1 antibody
RabMAbs
1 antibody
MyBioSource
4 antibodies
ProSci
1 antibody
St John's Laboratory
1 antibody
United States Biological
13 antibodies
Creative Diagnostics
2 antibodies
RayBiotech, Inc.
1 antibody