Gene: CNTLN
Alternate names for this Gene:
C9orf101|C9orf39|bA340N12.1
Gene Summary:
Gene is located in Chromosome:
9
Location in Chromosome :
9p22.2
Description of this Gene:
centlein
Type of Gene:
protein-coding
rs2779767
in
CNTLN
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.
rs2779772
in
CNTLN
gene and
Diabetes Mellitus, Non-Insulin-Dependent
PMID 21799836
2011 A genome-wide association study confirms previously reported loci for type 2 diabetes in Han Chinese.
rs10963012
in
CNTLN
gene and
High density lipoprotein measurement
PMID 30275531
2018 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
rs10963072
in
CNTLN
gene and
Leukemia, Myelocytic, Acute
PMID 27903959
2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
rs2779767
in
CNTLN
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.
rs10963067
in
CNTLN
gene and
Waist-Hip Ratio
PMID 30575882
2018 Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors.
PMID 30595370
2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.