Gene: UNC5D

Alternate names for this Gene: PRO34692|Unc5h4

Gene Summary:

Gene is located in Chromosome: 8

Location in Chromosome : 8p12

Description of this Gene: unc-5 netrin receptor D

Type of Gene: protein-coding

rs1528706 in UNC5D gene and Adolescent idiopathic scoliosis PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs6468316 in UNC5D gene and Blood Protein Measurement PMID 30072576 2018 Co-regulatory networks of human serum proteins link genetics to disease.

rs28485846 in UNC5D gene and Diabetes Mellitus, Insulin-Dependent PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs28485846 in UNC5D gene and Diabetes Mellitus, Non-Insulin-Dependent PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs28485846 in UNC5D gene and Diabetic Foot PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs28485846 in UNC5D gene and Hereditary and idiopathic neuropathy, unspecified PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs28485846 in UNC5D gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs28485846 in UNC5D gene and NEUROPATHY, CONGENITAL HYPOMYELINATING, 3 PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs16875831 in UNC5D gene and Narcolepsy PMID 19629137 2009 Genome-wide association database developed in the Japanese Integrated Database Project.

rs28485846 in UNC5D gene and Neuropathy PMID 28672053 2017 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers.

rs1528706 in UNC5D gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs13280010 in UNC5D gene and mathematical ability PMID 30038396 2018 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.