UGT2B7 UDP glucuronosyltransferase family 2 member B7
Information
- Symbol
- UGT2B7
- Type
- protein-coding
- Description
- UDP glucuronosyltransferase family 2 member B7
- Entrez Gene ID
- 7364
- Genome
- hg19
- Position
- chr4:69,962,192-69,978,705
- Genome
- hg38
- Position
- chr4:69,096,474-69,112,987
- MIM
- 600068 OMIM
- HGNC
- HGNC:12554 HGNC
- Ensembl
- ENSG00000171234 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
drug response | 0 | 232 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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232 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | UDPGT 2B7 |
SYNONYM | UDPGT 2B9 |
SYNONYM | UDPGT2B7 |
SYNONYM | UDPGTH2 |
SYNONYM | UDPGTh-2 |
SYNONYM | UGT2B9 |
MIM | 600068 OMIM |
HGNC | HGNC:12554 HGNC |
Ensembl | ENSG00000171234 Ensembl |
AllianceGenome | HGNC:12554 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000622664.1 | hg38 | chr4 | 69,096,519 | 69,112,984 | 16,466 |
ENST00000305231.12 | hg38 | chr4 | 69,096,474 | 69,112,987 | 16,514 |
ENST00000508661.5 | hg38 | chr4 | 69,096,494 | 69,112,972 | 16,479 |
ENST00000305231.12 | hg19 | chr4 | 69,962,192 | 69,978,705 | 16,514 |
ENST00000508661.5 | hg19 | chr4 | 69,962,212 | 69,978,690 | 16,479 |
ENST00000622664.1 | hg19 | chr4 | 69,962,237 | 69,978,702 | 16,466 |
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