Gene: LINC02210

Alternate names for this Gene: C17orf69|CRHR1-IT1

Gene Summary:

Gene is located in Chromosome: 17

Location in Chromosome : 17q21.31

Description of this Gene: long intergenic non-protein coding RNA 2210

Type of Gene: ncRNA

Gene: LINC02210-CRHR1

Alternate names for this Gene: CRHR1-IT1-CRHR1|MGC57346-CRHR1

Gene Summary: This locus represents naturally occurring readthrough transcription between neighboring genes CRHR1-IT1, CRHR1 intronic transcript 1 (Gene ID: 147081) and CRHR1, corticotropin releasing hormone receptor 1 (Gene ID: 1394) on chromosome 17. The readthrough transcript encodes a protein that shares sequence identity with the product of the CRHR1 gene.

Gene is located in Chromosome: 17

Location in Chromosome : 17q21.31

Description of this Gene: LINC02210-CRHR1 readthrough

Type of Gene: protein-coding

rs241036 in LINC02210;LINC02210-CRHR1 gene and Age at menarche PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs675600 in LINC02210;LINC02210-CRHR1 gene and Blood basophil count (lab test) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs142742547 in LINC02210;LINC02210-CRHR1 gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs393152 in LINC02210;LINC02210-CRHR1 gene and Corticobasal degeneration PMID 26077951 2015 Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.

rs675600 in LINC02210;LINC02210-CRHR1 gene and Eosinophil count procedure PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs675600 in LINC02210;LINC02210-CRHR1 gene and Granulocyte count PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs393152 in LINC02210;LINC02210-CRHR1 gene and Lung Diseases, Interstitial PMID 23583980 2013 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

rs675600 in LINC02210;LINC02210-CRHR1 gene and Neutrophil count (procedure) PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs241041 in LINC02210;LINC02210-CRHR1 gene and Parkinson Disease PMID 22438815 2012 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

PMID 21738487 2011 Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.

PMID 19915575 2009 Genome-wide association study reveals genetic risk underlying Parkinson's disease.

PMID 24842889 2014 Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

PMID 21044948 2011 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

rs241041 in LINC02210;LINC02210-CRHR1 gene and Primary biliary cirrhosis PMID 22961000 2012 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.

rs393152 in LINC02210;LINC02210-CRHR1 gene and Prion Diseases PMID 22210626 2012 Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.