ALDH3B2 aldehyde dehydrogenase 3 family member B2
Information
- Symbol
- ALDH3B2
- Type
- protein-coding
- Description
- aldehyde dehydrogenase 3 family member B2
- Entrez Gene ID
- 222
- Genome
- hg19
- Position
- chr11:67,429,626-67,442,094
- Genome
- hg38
- Position
- chr11:67,662,155-67,674,623
- MIM
- 601917 OMIM
- HGNC
- HGNC:411 HGNC
- Ensembl
- ENSG00000132746 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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68 |
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0 |
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
Search Word
Target data | : |
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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | ALDH8 |
MIM | 601917 OMIM |
HGNC | HGNC:411 HGNC |
Ensembl | ENSG00000132746 Ensembl |
AllianceGenome | HGNC:411 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000349015.7 | hg38 | chr11 | 67,662,163 | 67,674,631 | 12,469 |
ENST00000673966.2 | hg38 | chr11 | 67,662,155 | 67,674,623 | 12,469 |
ENST00000530069.6 | hg38 | chr11 | 67,662,160 | 67,681,224 | 19,065 |
ENST00000673966.2 | hg19 | chr11 | 67,429,626 | 67,442,094 | 12,469 |
ENST00000530069.6 | hg19 | chr11 | 67,429,631 | 67,448,695 | 19,065 |
ENST00000349015.7 | hg19 | chr11 | 67,429,634 | 67,442,102 | 12,469 |
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