chr13:30713478:> Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr13:31,287,615-31,338,563 |
| hg38 | chr13:30,713,478-30,764,426 |
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 | Cardiovascular Diseases | NA | BeFree | Detail | |
| 0.002 | Carotid Artery Diseases | NA | GAD | Detail | |
| 0.122 | cerebral infarction | NA | BeFree,CTD_human | Detail | |
| 0.012 | brain ischemia | NA | GAD | Detail | |
| 0.002 | cerebral palsy | NA | GAD | Detail | |
| 0.002 | Cerebrovascular Disorders | NA | GAD | Detail | |
| 0.005 | Coronary Arteriosclerosis | NA | BeFree,GAD | Detail | |
| 0.009 | Coronary heart disease | NA | BeFree,GAD | Detail | |
| 0.003 | Mental Depression | NA | BeFree,GAD | Detail | |
| <0.001 | depressive disorder | NA | BeFree | Detail | |
| 0.002 | generalized atherosclerosis | NA | GAD | Detail | |
| 0.080 | glomerulonephritis | NA | RGD | Detail | |
| 0.120 | IgA glomerulonephritis | NA | CTD_human | Detail | |
| 0.002 | Graft Occlusion, Vascular | NA | GAD | Detail | |
| <0.001 | HIV Infections | NA | BeFree | Detail | |
| 0.008 | Hypercholesterolemia, Familial | NA | BeFree,GAD | Detail | |
| 0.002 | Hypersensitivity | NA | GAD | Detail | |
| 0.002 | Hypertensive disease | NA | GAD | Detail | |
| 0.080 | pulmonary hypertension | NA | RGD | Detail | |
| 0.082 | Inflammation | NA | GAD,RGD | Detail | |
| 0.120 | Liver diseases | NA | CTD_human | Detail | |
| 0.080 | Mammary Neoplasms, Experimental | NA | RGD | Detail | |
| 0.027 | myocardial infarction | NA | BeFree,GAD,LHGDN | Detail | |
| 0.004 | Ischemic Cerebrovascular Accident | To investigate whether single nucleotide polymorphisms (SNPs) of eicosanoid bios... | BeFree | 21816595 | Detail |
| 0.009 | Ischemic stroke | To investigate whether single nucleotide polymorphisms (SNPs) of eicosanoid bios... | BeFree | 21816595 | Detail |
| <0.001 | obesity | NA | BeFree | Detail | |
| 0.120 | proteinuria | NA | CTD_human | Detail | |
| 0.002 | rhinitis | NA | GAD | Detail | |
| 0.002 | sinusitis | NA | GAD | Detail | |
| 0.115 | Cerebrovascular accident | Previous studies have implicated that two at-risk haplotypes (HapA and HapB) of ... | BeFree,GAD,LHGDN,RGD | 24198186 | Detail |
| <0.001 | pigmented villonodular synovitis | NA | BeFree | Detail | |
| 0.002 | Tobacco use disorder | NA | GAD | Detail | |
| 0.002 | xanthomatosis | NA | GAD | Detail | |
| <0.001 | Arterial thrombosis | NA | BeFree | Detail | |
| 0.120 | Neurotoxicity Syndromes | NA | CTD_human | Detail | |
| <0.001 | Thrombotic stroke | NA | BeFree | Detail | |
| 0.080 | Hyperoxia | NA | RGD | Detail | |
| <0.001 | Xanthoma | NA | BeFree | Detail | |
| <0.001 | Restenosis | NA | BeFree | Detail | |
| 0.002 | Metabolic syndrome X | NA | GAD | Detail | |
| 0.009 | Ischemic stroke | A novel risk haplotype of ALOX5AP gene is associated with ischemic stroke in Chi... | BeFree,GAD | 24198186 | Detail |
| 0.005 | Acute coronary syndrome | Interrelationships between ALOX5AP polymorphisms, serum leukotriene B4 level and... | BeFree,GAD | 25210744 | Detail |
| 0.002 | coronary restenosis | NA | GAD | Detail | |
| <0.001 | pancreatic ductal adenocarcinoma | NA | BeFree | Detail | |
| <0.001 | Coronary heart disease, susceptibility to, 5 | NA | BeFree | Detail | |
| 0.004 | Ischemic Cerebrovascular Accident | A novel risk haplotype of ALOX5AP gene is associated with ischemic stroke in Chi... | BeFree | 24198186 | Detail |
| <0.001 | Allergic disposition | NA | BeFree | Detail | |
| <0.001 | adenoma | NA | BeFree | Detail | |
| 0.002 | Alzheimer's disease | NA | GAD | Detail | |
| 0.003 | Anoxia | NA | LHGDN | Detail | |
| <0.001 | aortic aneurysm | NA | BeFree | Detail | |
| 0.002 | arteriosclerosis | The eicosanoid genes ALOX5, ALOX5AP and LTA4H have been implicated in atheroscle... | BeFree | 25721704 | Detail |
| 0.024 | asthma | NA | BeFree,GAD,LHGDN | Detail | |
| 0.134 | atherosclerosis | The eicosanoid genes ALOX5, ALOX5AP and LTA4H have been implicated in atheroscle... | BeFree,CTD_human,GAD | 25721704 | Detail |
| <0.001 | Rectal Carcinoma | NA | BeFree | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| 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 |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| To investigate whether single nucleotide polymorphisms (SNPs) of eicosanoid biosynthesis genes are a... | DisGeNET | Detail |
| To investigate whether single nucleotide polymorphisms (SNPs) of eicosanoid biosynthesis genes are a... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| Previous studies have implicated that two at-risk haplotypes (HapA and HapB) of gene-encoding 5-lipo... | 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 |
| A novel risk haplotype of ALOX5AP gene is associated with ischemic stroke in Chinese Han population. | DisGeNET | Detail |
| Interrelationships between ALOX5AP polymorphisms, serum leukotriene B4 level and risk of acute coron... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| A novel risk haplotype of ALOX5AP gene is associated with ischemic stroke in Chinese Han population. | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| The eicosanoid genes ALOX5, ALOX5AP and LTA4H have been implicated in atherosclerosis. | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| The eicosanoid genes ALOX5, ALOX5AP and LTA4H have been implicated in atherosclerosis. | 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
- -
- dbSNP
- rs386592567 dbSNP
- Genome
- hg38
- Position
- chr13:30,713,478-30,764,426
- Variant Type
- snv
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