rs10427132
This is a intron variant variant in the MYO9B gene.
▶GWAS Catalog Trait Associations (13)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (13)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
free cholesterol to total lipids in very large VLDL percentage
total lipids in medium VLDL
free cholesterol to total lipids in medium VLDL percentage
cholesteryl esters to total lipids in large VLDL percentage
triglycerides to total lipids in medium VLDL percentage
cholesterol to total lipids in medium VLDL percentage
triglycerides to total lipids in very large VLDL percentage
cholesterol to total lipids in small VLDL percentage
cholesteryl ester measurement
triglycerides to total lipids in small VLDL percentage
About MYO9B
This gene encodes a member of the myosin family of actin-based molecular motor heavy chain proteins. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-9 (MYH9). The protein has four IQ motifs located in the neck domain that bind calmodulin, which serves as a light chain. The protein complex has a single-headed structure and exhibits processive movement on actin filaments toward the minus-end. The protein also has rho-GTPase activity. Polymorphisms in this gene are associated with celiac disease and ulcerative colitis susceptibility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
View all MYO9B variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
Community Wiki
No community notes yet for this variant. Sign in to start one.
Comments
Sign in to join the discussion.
Loading comments…