chr21:44473301:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr21:44,473,301-44,496,488
hg38 chr21:43,053,191-43,076,378 

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
0.127 Cardiovascular Diseases NA BeFree,CTD_human,GAD,LHGDN Detail
0.003 intracranial aneurysm NA BeFree,GAD Detail
<0.001 cerebral infarction NA BeFree Detail
0.005 brain ischemia NA GAD Detail
0.005 cerebral palsy NA GAD Detail
0.002 Cerebrovascular Disorders NA GAD Detail
0.005 cleft lip NA GAD Detail
0.005 cleft palate NA GAD Detail
<0.001 Cognition Disorders Polymorphisms of genes involved in B vitamin absorption, metabolism and function... BeFree 25173634 Detail
<0.001 colorectal carcinoma Effect of S-adenosyl-L-methionine (SAM), an allosteric activator of cystathionin... BeFree 24667534 Detail
0.002 Colorectal Neoplasms NA GAD Detail
0.003 Connective Tissue Diseases NA BeFree,GAD Detail
0.006 Coronary Arteriosclerosis NA BeFree,GAD Detail
0.008 Coronary heart disease NA BeFree,GAD Detail
0.003 Demyelinating Diseases NA LHGDN Detail
<0.001 Mental Depression We observed a significant reduction in sulphide concentrations and downregulated... BeFree 25070356 Detail
<0.001 depressive disorder We observed a significant reduction in sulphide concentrations and downregulated... BeFree 25070356 Detail
<0.001 dermatitis NA BeFree Detail
<0.001 Diabetes NA BeFree Detail
<0.001 diabetes mellitus NA BeFree Detail
0.122 Diabetes Mellitus, Non-Insulin-Dependent NA CTD_human,GAD Detail
0.024 Down syndrome NA BeFree,GAD,LHGDN Detail
0.002 Edema NA GAD Detail
<0.001 Fatty Liver NA BeFree Detail
0.002 Fetal Diseases NA GAD Detail
<0.001 Folic Acid Deficiency NA BeFree Detail
0.010 congenital heart defects NA BeFree,GAD Detail
0.003 Heart Diseases NA LHGDN Detail
0.002 Heart Septal Defects NA GAD Detail
0.156 homocystinuria Altered hepatic sulfur metabolism in cystathionine β-synthase-deficient homocyst... BeFree,CTD_human,GAD,LHGDN 24891521 Detail
0.003 Huntington disease NA BeFree,GAD Detail
0.122 Hypertensive disease NA CTD_human,GAD Detail
<0.001 Immunologic Deficiency Syndromes NA BeFree Detail
0.007 Inflammation NA GAD Detail
<0.001 Inflammatory Bowel Diseases NA BeFree Detail
<0.001 leukemia NA BeFree Detail
<0.001 Leukemia, Lymphocytic, Acute, L1 NA BeFree Detail
0.003 Acute Megakaryocytic Leukemias NA BeFree,LHGDN Detail
<0.001 Leukemia, Myelocytic, Acute NA BeFree Detail
0.003 liver cirrhosis NA BeFree,GAD Detail
<0.001 Liver neoplasms NA BeFree Detail
0.002 Chronic Obstructive Airway Disease NA GAD Detail
0.005 Lung Neoplasms NA BeFree,GAD,LHGDN Detail
0.002 Lupus Erythematosus, Systemic NA GAD Detail
0.002 lymphoma NA GAD Detail
0.002 Lymphoma, Follicular NA GAD Detail
0.128 Lymphoma, Non-Hodgkin Our study suggests that variation in several OCM genes (CBS, FTHFD, SHMT1, TCN1,... BeFree,CTD_human,GAD 25384508 Detail
<0.001 Malignant neoplasm of stomach NA BeFree Detail
0.005 meningioma NA BeFree,GAD,LHGDN Detail
<0.001 Meningomyelocele NA BeFree Detail
0.008 Mental Retardation NA BeFree,GAD Detail
0.004 Inborn errors of metabolism NA BeFree,LHGDN Detail
<0.001 multiple myeloma NA BeFree Detail
0.002 Musculoskeletal Diseases NA GAD Detail
<0.001 Mycoses NA BeFree Detail
0.010 myocardial infarction NA BeFree,GAD Detail
0.007 Neural Tube Defects NA GAD Detail
0.003 obesity NA BeFree,GAD Detail
<0.001 ovarian carcinoma NA BeFree Detail
0.002 Parkinson disease NA GAD Detail
<0.001 Adenomatous Polyposis Coli NA BeFree Detail
<0.001 Preexcitation Syndrome NA BeFree Detail
0.002 Pregnancy Complications, Hematologic NA GAD Detail
0.002 Prostatic Neoplasms NA GAD Detail
<0.001 pyruvate carboxylase deficiency disease NA BeFree Detail
<0.001 Renal Artery Stenosis NA BeFree Detail
<0.001 kidney failure NA BeFree Detail
0.024 Down syndrome In the present study, we determined polymorphisms of MTHFR A222V (677C &gt; T), ... BeFree 15889417 Detail
0.003 schizophrenia NA BeFree,GAD Detail
<0.001 Septicemia NA BeFree Detail
<0.001 Sinus Thrombosis, Intracranial NA BeFree Detail
0.002 Dermatologic disorders NA GAD Detail
0.002 Stomach Neoplasms NA GAD Detail
0.006 Cerebrovascular accident Therefore, CBS inhibition may be a viable approach to stroke treatment. BeFree,GAD 25873304 Detail
<0.001 Subarachnoid Hemorrhage NA BeFree Detail
0.002 Thromboembolism NA BeFree Detail
0.002 Tobacco use disorder NA GAD Detail
0.002 Vascular Diseases NA BeFree Detail
0.005 Venous Thrombosis NA GAD Detail
0.002 B-Cell Lymphomas NA GAD Detail
0.002 diffuse large B-cell lymphoma NA GAD Detail
<0.001 Lymphoma, Large-Cell, Follicular NA BeFree Detail
0.002 T-Cell Lymphoma NA GAD Detail
0.012 spina bifida NA BeFree,GAD Detail
0.002 Central Nervous System Neoplasms NA GAD Detail
0.003 Deep Vein Thrombosis NA BeFree,GAD Detail
0.009 Premature Birth NA GAD Detail
0.003 Thrombosis of cerebral veins NA BeFree,GAD Detail
0.003 adrenoleukodystrophy NA BeFree,LHGDN Detail
0.123 Malnutrition NA BeFree,CTD_human,GAD Detail
0.002 Aortic Aneurysm, Abdominal NA GAD Detail
<0.001 Russell-Silver syndrome Interestingly, patients with RSS with ICR1 hypomethylation showed uneven profile... BeFree 25395389 Detail
0.002 coronary stenosis NA GAD Detail
0.007 Malignant neoplasm of lung NA BeFree,GAD Detail
0.002 age related macular degeneration NA GAD Detail
<0.001 Sepsis NA BeFree Detail
<0.001 Malignant neoplasm of colon stage IV NA BeFree Detail
<0.001 Cancer of Head and Neck NA BeFree Detail
0.328 Cystathionine beta-Synthase Deficiency Disease Effect of the disease-causing R266K mutation on the heme and PLP environments of... UNIPROT 22738154 Detail
0.002 Restenosis NA GAD Detail
0.002 Vertebral Artery Dissection NA GAD Detail
<0.001 Impaired cognition NA BeFree Detail
<0.001 Malignant neoplasm of prostate NA BeFree Detail
0.003 thrombophilia NA BeFree,GAD Detail
<0.001 Neurodegenerative Disorders A significant reduction in sulphide levels and CBS mRNA expression was observed ... BeFree 24874797 Detail
0.002 Methotrexate poisoning NA GAD Detail
<0.001 Factor V Leiden mutation NA BeFree Detail
0.229 hyperhomocysteinemia Mild (22 µmol/L) and moderate (88 µmol/L) HHcy were induced in cystathionine β-s... BeFree,CTD_human,GAD,LHGDN,RGD 25352635 Detail
0.229 hyperhomocysteinemia We studied the effect of HHcy on PCs and its role in vascular repair in severe H... BeFree,CTD_human,GAD,LHGDN,RGD 25854700 Detail
<0.001 Leukemogenesis NA BeFree Detail
<0.001 prostate carcinoma NA BeFree Detail
0.002 Activated Protein C Resistance NA GAD Detail
0.002 hepatopulmonary syndrome NA GAD Detail
<0.001 Epithelial ovarian cancer NA BeFree Detail
<0.001 breast carcinoma NA BeFree Detail
<0.001 Carcinoma of lung NA BeFree Detail
<0.001 Malignant neoplasm of gastrointestinal tract NA BeFree Detail
0.002 Chronic progressive chorea NA GAD Detail
0.003 colon carcinoma The purpose of the current study was to investigate the effect of the allosteric... BeFree 24667534 Detail
0.003 colon carcinoma Here, we compare the effectiveness of Ca(2+), vitamin D, and Aquamin (a marine a... BeFree 26076051 Detail
<0.001 stomach carcinoma NA BeFree Detail
<0.001 Carcinoma of bladder NA BeFree Detail
0.002 Carotid Artery, Internal, Dissection NA GAD Detail
0.007 brain infarction NA GAD Detail
<0.001 Arteriopathic disease NA BeFree Detail
<0.001 Endothelial dysfunction NA BeFree Detail
0.024 Down syndrome We concluded that RFC-1 and CBS gene mutation alleles are related to Down syndro... BeFree 23430030 Detail
<0.001 Cerebral Ischemia NA BeFree Detail
<0.001 ovarian neoplasm NA BeFree Detail
<0.001 Ischemic stroke NA BeFree Detail
<0.001 Malignant neoplasm of ovary NA BeFree Detail
0.013 colorectal cancer Effect of S-adenosyl-L-methionine (SAM), an allosteric activator of cystathionin... BeFree,GAD 24667534 Detail
<0.001 Renal Insufficiency NA BeFree Detail
<0.001 Meningioma, benign, no ICD-O subtype NA BeFree Detail
0.014 coronary artery disease NA BeFree,GAD,LHGDN Detail
0.001 liver carcinoma NA BeFree Detail
<0.001 Steatohepatitis NA BeFree Detail
<0.001 Ischemic Cerebrovascular Accident NA BeFree Detail
0.089 Homocysteinemia In this review we highlight the importance of homocysteinemia by describing the ... BeFree,MGD 25087163 Detail
0.089 Homocysteinemia Mild (22 µmol/L) and moderate (88 µmol/L) HHcy were induced in cystathionine β-s... BeFree,MGD 25352635 Detail
0.089 Homocysteinemia We studied the effect of HHcy on PCs and its role in vascular repair in severe H... BeFree,MGD 25854700 Detail
0.001 Homocystinuria, pyridoxine-responsive NA BeFree Detail
0.002 Infection NA GAD Detail
<0.001 intellectual disability We present diagnosis of cystathionine beta-synthase (CBS) deficiency in a multip... BeFree 25455305 Detail
0.005 Hyperhomocystinemia NA GAD Detail
0.002 Congenital Abnormality NA GAD Detail
0.002 adenocarcinoma NA GAD Detail
0.010 Alzheimer's disease NA BeFree,GAD,LHGDN Detail
<0.001 Aneurysm, Dissecting NA BeFree Detail
<0.001 Arterial Occlusive Diseases NA BeFree Detail
0.001 arteriosclerosis NA BeFree Detail
0.006 atherosclerosis NA BeFree,GAD Detail
0.005 Malignant neoplasm of urinary bladder NA BeFree,GAD Detail
0.002 Brain Neoplasms NA GAD Detail
0.007 Malignant neoplasm of breast NA BeFree,GAD Detail
<0.001 oral candidiasis NA BeFree Detail
<0.001 Malignant tumor of colon The purpose of the current study was to investigate the effect of the allosteric... BeFree 24667534 Detail
0.002 Non-small cell lung carcinoma NA GAD Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
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Polymorphisms of genes involved in B vitamin absorption, metabolism and function, such as methylene ... DisGeNET Detail
Effect of S-adenosyl-L-methionine (SAM), an allosteric activator of cystathionine-β-synthase (CBS) o... DisGeNET Detail
NA DisGeNET Detail
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We observed a significant reduction in sulphide concentrations and downregulated expression of cysta... DisGeNET Detail
We observed a significant reduction in sulphide concentrations and downregulated expression of cysta... DisGeNET Detail
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Altered hepatic sulfur metabolism in cystathionine β-synthase-deficient homocystinuria: regulatory r... DisGeNET Detail
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Our study suggests that variation in several OCM genes (CBS, FTHFD, SHMT1, TCN1, and TYMS) may influ... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
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In the present study, we determined polymorphisms of MTHFR A222V (677C &gt; T), MTHFR E429A (1298A &... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
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Therefore, CBS inhibition may be a viable approach to stroke treatment. DisGeNET Detail
NA DisGeNET Detail
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NA DisGeNET Detail
NA DisGeNET Detail
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Interestingly, patients with RSS with ICR1 hypomethylation showed uneven profiles of methylation amo... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Effect of the disease-causing R266K mutation on the heme and PLP environments of human cystathionine... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
A significant reduction in sulphide levels and CBS mRNA expression was observed in the hippocampus o... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Mild (22 µmol/L) and moderate (88 µmol/L) HHcy were induced in cystathionine β-synthase wild-type (C... DisGeNET Detail
We studied the effect of HHcy on PCs and its role in vascular repair in severe HHcy (∼150 μM), which... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
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The purpose of the current study was to investigate the effect of the allosteric CBS activator S-ade... DisGeNET Detail
Here, we compare the effectiveness of Ca(2+), vitamin D, and Aquamin (a marine algae product contain... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
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We concluded that RFC-1 and CBS gene mutation alleles are related to Down syndrome, and women with m... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
Effect of S-adenosyl-L-methionine (SAM), an allosteric activator of cystathionine-β-synthase (CBS) o... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
In this review we highlight the importance of homocysteinemia by describing the genes encoding for e... DisGeNET Detail
Mild (22 µmol/L) and moderate (88 µmol/L) HHcy were induced in cystathionine β-synthase wild-type (C... DisGeNET Detail
We studied the effect of HHcy on PCs and its role in vascular repair in severe HHcy (∼150 μM), which... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We present diagnosis of cystathionine beta-synthase (CBS) deficiency in a multiply affected Iranian ... DisGeNET Detail
NA DisGeNET Detail
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The purpose of the current study was to investigate the effect of the allosteric CBS activator S-ade... DisGeNET Detail
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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
rs28934275 dbSNP
Genome
hg19
Position
chr21:44,473,301-44,496,488
Variant Type
snv
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