CLDN19

gene product
The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jun 2010]
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Novus Biologicals
3 antibodies
Cusabio Biotech Co., Ltd
4 antibodies
Affinity Biosciences
1 antibody
antibodies-online
61 antibodies
LifeSpan BioSciences, Inc.
24 antibodies
OriGene
4 antibodies
R&D Systems
1 antibody
Biorbyt
14 antibodies
Invitrogen Antibodies
4 antibodies
Aviva Systems Biology
2 antibodies
Abnova Corporation
3 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
GeneTex
1 antibody
Boster Biological Technology
2 antibodies
St John's Laboratory
2 antibodies
Abbexa
6 antibodies
NovoPro Bioscience Inc.
1 antibody
Creative Diagnostics
2 antibodies
MyBioSource
5 antibodies
Creative Biolabs
3 antibodies
RayBiotech, Inc.
1 antibody
Abgent
1 antibody
Leading Biology
1 antibody
MilliporeSigma / Merck KGaA
1 antibody