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CNTN4 encodes a member of the contactin family of immunoglobulins. Additionally we are shipping Contactin 4 Antibodies (37) and Contactin 4 Kits (25) and many more products for this protein.
Showing 7 out of 8 products:
Human Contactin 4 Protein expressed in Baculovirus infected Insect Cells - ABIN2002259
Fernandez, Morgan, Davis, Klin, Morris, Farhi, Lifton, State: Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. in American journal of human genetics 2004
SNPs in ITPR1 (show ITPR1 Proteins) and CNTN4 are involved in the regulation of serum uric acid concentrations in Mexican Americans
By combining methylation and SNP data, CNTN4 was identified as a risk factor for regular alcohol use.
data reveal critical and novel roles for CNTN4/amyloid precursor protein (show APP Proteins) in promoting target-specific axon arborization
We identified CNTN4 as a novel candidate gene for POAG.
these results suggest that rare copy number variations in CNTN4 may also influence autism susceptibility in Asian populations.
Using array comparative genome hybridization (CGH), we identified a maternally inherited approximately 535 kb deletion at 3p26.3 encompassing the 5' end of the contactin 4 gene (CNTN4) in a patient with autism.
Our results demonstrate the association of CNTN4 disruption with the 3p deletion syndrome phenotype and strongly suggest a causal relationship
The contactin 4 gene (CNTN4) is associated with cerebellar degeneration in spinocerebellar ataxia (show USP14 Proteins) type 16. Additional studies are necessary to prove 4,256C-->T to be a causative mutation.
pathological examinations and molecular biological examinations are needed to confirm that this mutation is a true cause of SCA16 (show ITPR1 Proteins)
This report suggests that mutations affecting CNTN4 function may be relevant to Autism spectrum disorder pathogenesis.
including the adhesion molecule (show NCAM1 Proteins) CNTN4,which contributed to the enhanced response
These results suggest that BIG-2 is one of the axon guidance molecules crucial for the formation and maintenance of functional odor map in the olfactory bulb.
This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants.
, axonal-associated cell adhesion molecule
, brain-derived immunoglobulin superfamily protein 2
, neural cell adhesion protein BIG-2
, brain-derived immunoglobulin superfamily molecule
, FAR-1 protein fragment