chr4:69512315:> Detail (hg19)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr4:69,512,315-69,536,370 |
hg38 | chr4:68,646,597-68,670,652 |
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 | colorectal carcinoma | NA | BeFree | Detail | |
0.002 | Deafness | NA | GAD | Detail | |
<0.001 | Diabetes Mellitus, Non-Insulin-Dependent | NA | BeFree | Detail | |
0.002 | Duodenal Neoplasms | NA | GAD | Detail | |
0.002 | Gilbert Disease (disorder) | NA | GAD | Detail | |
0.002 | Hearing Loss, Partial | NA | GAD | Detail | |
0.002 | Insulin resistance | NA | GAD | Detail | |
<0.001 | Rectal Carcinoma | A haplotype in UGT2B15 containing a functional variant (rs4148269, K523T) and an... | BeFree | 24822274 | Detail |
<0.001 | melanoma | NA | BeFree | Detail | |
0.002 | Adenomatous Polyposis Coli | NA | GAD | Detail | |
0.128 | Prostatic Neoplasms | NA | BeFree,CTD_human,LHGDN | Detail | |
<0.001 | Tumor Progression | NA | BeFree | Detail | |
<0.001 | Metastatic melanoma | NA | BeFree | Detail | |
0.002 | Malignant neoplasm of liver | NA | GAD | Detail | |
0.016 | Malignant neoplasm of prostate | Regulation of Human UGT2B15 and UGT2B17 by miR-376c in Prostate Cancer Cell Line... | BeFree,GAD | 26163549 | Detail |
0.004 | prostate carcinoma | Regulation of Human UGT2B15 and UGT2B17 by miR-376c in Prostate Cancer Cell Line... | BeFree | 26163549 | Detail |
0.001 | breast carcinoma | As 4-OHTAM is a UGT2B15 substrate, the upregulation of UGT2B15 by 4-OHTAM in tar... | BeFree | 25795461 | Detail |
<0.001 | Secondary malignant neoplasm of lymph node | NA | BeFree | Detail | |
0.002 | Mammographic breast density | NA | GAD | Detail | |
<0.001 | Hormone refractory prostate cancer | NA | BeFree | Detail | |
0.002 | hearing impairment | NA | GAD | Detail | |
0.003 | Mammary Neoplasms | NA | LHGDN | Detail | |
<0.001 | colorectal cancer | NA | BeFree | Detail | |
0.002 | Hearing Loss | NA | GAD | Detail | |
0.008 | Malignant neoplasm of breast | As 4-OHTAM is a UGT2B15 substrate, the upregulation of UGT2B15 by 4-OHTAM in tar... | BeFree,GAD | 25795461 | 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 |
A haplotype in UGT2B15 containing a functional variant (rs4148269, K523T) and an intronic SNP (rs683... | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
Regulation of Human UGT2B15 and UGT2B17 by miR-376c in Prostate Cancer Cell Lines. | DisGeNET | Detail |
Regulation of Human UGT2B15 and UGT2B17 by miR-376c in Prostate Cancer Cell Lines. | DisGeNET | Detail |
As 4-OHTAM is a UGT2B15 substrate, the upregulation of UGT2B15 by 4-OHTAM in target breast cancer ce... | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
NA | DisGeNET | Detail |
As 4-OHTAM is a UGT2B15 substrate, the upregulation of UGT2B15 by 4-OHTAM in target breast cancer ce... | 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
- rs148447518 dbSNP
- Genome
- hg19
- Position
- chr4:69,512,315-69,536,370
- Variant Type
- snv
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