ALKBH5 alkB homolog 5, RNA demethylase
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 2 | 0 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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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
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 |
Search Word
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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Search word | : | |
Filtering | : |
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 |
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SYNONYM | ABH5 |
SYNONYM | OFOXD |
SYNONYM | OFOXD1 |
MIM | 613303 OMIM |
HGNC | HGNC:25996 HGNC |
Ensembl | ENSG00000091542 Ensembl |
AllianceGenome | HGNC:25996 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000541285.1 | hg38 | chr17 | 18,183,078 | 18,209,398 | 26,321 |
ENST00000399138.5 | hg38 | chr17 | 18,183,828 | 18,209,954 | 26,127 |
ENST00000541285.1 | hg19 | chr17 | 18,086,392 | 18,112,712 | 26,321 |
ENST00000399138.5 | hg19 | chr17 | 18,087,142 | 18,113,268 | 26,127 |
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