rs6590207
This is a intron variant variant in the KIRREL3 gene.
▶GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (7)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
level of adhesion G protein-coupled receptor E1 in blood
CD86 molecule level
macrophage colony-stimulating factor 1 receptor level
level of receptor-type tyrosine-protein phosphatase C in blood
CD80 molecule level
CUB domain-containing protein 1 measurement
high density lipoprotein cholesterol measurement
About KIRREL3
The protein encoded by this gene is a member of the nephrin-like protein family. These proteins are expressed in fetal and adult brain, and also in podocytes of kidney glomeruli. The cytoplasmic domains of these proteins interact with the C-terminus of podocin, also expressed in the podocytes, cells involved in ensuring size- and charge-selective ultrafiltration. The protein encoded by this gene is a synaptic cell adhesion molecule with multiple extracellular immunoglobulin-like domains and a cytoplasmic PDZ domain-binding motif. Mutations in this gene are associated with several neurological and cognitive disorders. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
View all KIRREL3 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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