chr22:24819565:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr22:24,819,565-24,838,325
hg38 chr22:24,423,597-24,442,357 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Cardiomyopathy, Dilated NA BeFree Detail
<0.001 Dementia, Vascular NA BeFree Detail
0.080 Diabetes Mellitus, Experimental NA RGD Detail
0.122 drug allergy NA CTD_human,GAD Detail
<0.001 Dyskinetic syndrome Is there a role for ADORA2A polymorphisms in levodopa-induced dyskinesia in Park... BeFree 25872644 Detail
<0.001 epidermodysplasia verruciformis NA BeFree Detail
0.002 Fatigue NA GAD Detail
0.003 Fibrosis NA LHGDN Detail
<0.001 Headache NA BeFree Detail
<0.001 Heart failure NA BeFree Detail
<0.001 congestive heart failure NA BeFree Detail
<0.001 Hodgkin Disease NA BeFree Detail
0.008 Huntington disease NA BeFree,GAD,LHGDN Detail
0.003 Hypertensive disease NA BeFree,GAD Detail
0.120 Hypotension NA CTD_human Detail
0.122 Sleep Initiation and Maintenance Disorders NA CTD_human,GAD Detail
0.003 ischemia NA LHGDN Detail
<0.001 Lesch-Nyhan syndrome NA BeFree Detail
0.120 Liver Cirrhosis, Experimental NA CTD_human Detail
0.080 Lung diseases NA RGD Detail
0.003 Chronic Obstructive Airway Disease NA LHGDN Detail
<0.001 myopia NA BeFree Detail
0.134 panic disorder NA BeFree,CTD_human,GAD,LHGDN Detail
0.003 Parkinson disease Increased striatal adenosine A2A receptor levels is an early event in Parkinson'... BeFree,GAD 24892887 Detail
0.122 Psychoses, Substance-Induced NA CTD_human,GAD Detail
0.080 Reperfusion Injury NA RGD Detail
0.004 schizophrenia NA BeFree,GAD Detail
<0.001 systemic scleroderma NA BeFree Detail
0.120 Seizures NA BeFree,CTD_human Detail
<0.001 status epilepticus NA BeFree Detail
0.120 Substance Withdrawal Syndrome NA CTD_human Detail
0.005 Syncope NA BeFree,GAD,LHGDN Detail
0.120 Tremor NA CTD_human Detail
0.120 Adverse reaction to drug NA CTD_human Detail
0.002 Weight Gain NA GAD Detail
<0.001 essential hypertension NA BeFree Detail
<0.001 Encephalopathies NA BeFree Detail
<0.001 Migraine Disorders NA BeFree Detail
<0.001 obstructive nephropathy NA BeFree Detail
<0.001 lingual-facial-buccal dyskinesia NA BeFree Detail
<0.001 migraine with aura NA BeFree Detail
<0.001 Renal interstitial fibrosis NA BeFree Detail
0.122 Amphetamine-Related Disorders NA CTD_human,GAD Detail
<0.001 Fibrosis, Liver NA BeFree Detail
0.120 Ventricular Dysfunction NA CTD_human Detail
<0.001 Carcinoma, Lewis Lung NA BeFree Detail
<0.001 Chronic heart failure The association of ADORA2A and ADORA2B polymorphisms with the risk and severity ... BeFree 25629231 Detail
<0.001 Solid tumour NA BeFree Detail
<0.001 Phobic anxiety disorder NA BeFree Detail
<0.001 Abnormal involuntary movement NA BeFree Detail
0.120 Hyperactive behavior NA CTD_human Detail
<0.001 Neurodegenerative Disorders Overall, these findings reveal that increased A2AR protein levels occur in asymp... BeFree 24892887 Detail
0.003 Mood Disorders NA BeFree,GAD Detail
<0.001 inflammatory joint disease NA BeFree Detail
<0.001 Tardive Dyskinesia NA BeFree Detail
0.002 Chronic progressive chorea NA GAD Detail
0.005 Sleep Disorders NA GAD Detail
0.120 Cardiomyopathies NA CTD_human Detail
<0.001 Sleeplessness NA BeFree Detail
<0.001 Autism Spectrum Disorders NA BeFree Detail
0.080 MYOPIA 2 (disorder) NA MGD Detail
0.002 PANIC DISORDER 1 NA BeFree Detail
0.002 Weight Gain Adverse Event NA GAD Detail
0.080 Idiopathic pulmonary arterial hypertension NA MGD Detail
<0.001 agoraphobia NA BeFree Detail
<0.001 Alzheimer's disease We found that humans with Alzheimer's disease (AD) had increased levels of the G... BeFree 25622143 Detail
0.125 Anxiety Disorders NA BeFree,CTD_human,GAD Detail
0.125 rheumatoid arthritis NA BeFree,CTD_human,GAD Detail
0.008 asthma NA GAD,LHGDN Detail
0.002 atherosclerosis NA GAD Detail
0.003 autistic disorder NA BeFree,GAD Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Is there a role for ADORA2A polymorphisms in levodopa-induced dyskinesia in Parkinson's disease pati... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Increased striatal adenosine A2A receptor levels is an early event in Parkinson's disease-related pa... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
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NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
The association of ADORA2A and ADORA2B polymorphisms with the risk and severity of chronic heart fai... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Overall, these findings reveal that increased A2AR protein levels occur in asymptomatic PD patients ... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We found that humans with Alzheimer's disease (AD) had increased levels of the Gs-coupled adenosine ... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chr22:24,819,565-24,838,325
Variant Type
snv
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