Gene: LINC00243
Alternate names for this Gene:
Gene Summary:
Gene is located in Chromosome:
Location in Chromosome :
Description of this Gene:
Type of Gene:
rs151302046 in
LINC00243 gene and
17 Hydroxyprogesterone measurement
PMID 31169883 2019 Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease.
rs13198118 in
LINC00243 gene and
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.
PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.
rs13198118 in
LINC00243 gene and
AIDS, PROGRESSION TO
PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.
PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.
rs886424 in
LINC00243 gene and
Adenocarcinoma of lung (disorder)
PMID 19836008 2009 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
rs3130783 in
LINC00243 gene and
Age related macular degeneration
PMID 23455636 2013 Seven new loci associated with age-related macular degeneration.
rs886424 in
LINC00243 gene and
Autoimmune thyroiditis
PMID 25936594 2015 Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.
rs886424 in
LINC00243 gene and
Bipolar Disorder
PMID 22688191 2012 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
rs1264347 in
LINC00243 gene and
Body Height
PMID 28552196 2017 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
rs4713376 in
LINC00243 gene and
Charcot-Marie-Tooth Disease, Type Ia (disorder)
PMID 30958311 2019 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.
rs114964506 in
LINC00243 gene and
Child Development Disorders, Pervasive
PMID 28540026 2017 Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
rs1264347 in
LINC00243 gene and
Diabetes
PMID 31451708 2019 Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
rs1264347 in
LINC00243 gene and
Diabetes Mellitus
PMID 31451708 2019 Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
rs1264350 in
LINC00243 gene and
Diabetes Mellitus, Insulin-Dependent
PMID 17632545 2007 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
PMID 25936594 2015 Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.
rs4587207 in
LINC00243 gene and
Duration of sleep
PMID 25469926 2015 Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study.
rs1264347 in
LINC00243 gene and
Glomerular Filtration Rate
PMID 31451708 2019 Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
rs13198118 in
LINC00243 gene and
HIV-1, RESISTANCE TO
PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.
PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.
rs13198118 in
LINC00243 gene and
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
PMID 21051598 2010 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.
PMID 20041166 2009 Common genetic variation and the control of HIV-1 in humans.
rs3130648 in
LINC00243 gene and
Hepatitis B
PMID 23760081 2013 A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
rs886424 in
LINC00243 gene and
Lupus Erythematosus, Systemic
PMID 24871463 2014 GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.
rs886424 in
LINC00243 gene and
Malignant neoplasm of lung
PMID 22899653 2012 Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
rs886424 in
LINC00243 gene and
Mental disorders
PMID 22688191 2012 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
rs3094123 in
LINC00243 gene and
Multiple Sclerosis
PMID 17660530 2007 Risk alleles for multiple sclerosis identified by a genomewide study.
rs886424 in
LINC00243 gene and
Myasthenia Gravis
PMID 23055271 2012 Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
rs886424 in
LINC00243 gene and
Psychotic Disorders
PMID 22688191 2012 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
rs12192704 in
LINC00243 gene and
Rheumatoid Arthritis
PMID 19503088 2009 REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.
PMID 17804836 2007 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.
rs114964506 in
LINC00243 gene and
Schizophrenia
PMID 28540026 2017 Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
PMID 30285260 2019 Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
PMID 22688191 2012 No single-nucleotide polymorphisms (SNPs) achieved significance in these new samples; however, combining new and previously reported SCZ samples (2111 SCZ and 2535 controls) revealed a genome-wide significant association in the major histocompatibility complex (MHC) region (rs886424, P=4.54 × 10(-8)).
rs1264350 in
LINC00243 gene and
Vitiligo
PMID 20526339 2010 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.