ALKBH8 alkB homolog 8, tRNA methyltransferase
Information
- Symbol
- ALKBH8
- Type
- protein-coding
- Description
- alkB homolog 8, tRNA methyltransferase
- Entrez Gene ID
- 91801
- Genome
- hg19
- Position
- chr11:107,373,453-107,436,461
- Genome
- hg38
- Position
- chr11:107,502,727-107,565,735
- MIM
- 613306 OMIM
- HGNC
- HGNC:25189 HGNC
- Ensembl
- ENSG00000137760 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 6 |
| Likely pathogenic | 0 | 8 |
| Benign | 0 | 30 |
| Likely benign | 0 | 32 |
| Conflicting classifications of pathogenicity | 0 | 8 |
| Uncertain significance | 0 | 96 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
36 |
 |
124 |
 |
4 |
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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| Category | : |
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | TRMT9A |
| SYNONYM | ABH8 |
| SYNONYM | MRT71 |
| SYNONYM | TRM9 |
| SYNONYM | TRMT9 |
| MIM | 613306 OMIM |
| HGNC | HGNC:25189 HGNC |
| Ensembl | ENSG00000137760 Ensembl |
| AllianceGenome | HGNC:25189 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000428149.7 | hg38 | chr11 | 107,502,727 | 107,565,735 | 63,009 |
| ENST00000389568.7 | hg38 | chr11 | 107,504,595 | 107,565,518 | 60,924 |
| ENST00000429370.5 | hg38 | chr11 | 107,503,029 | 107,565,735 | 62,707 |
| ENST00000417449.6 | hg38 | chr11 | 107,504,658 | 107,565,742 | 61,085 |
| ENST00000428149.7 | hg19 | chr11 | 107,373,453 | 107,436,461 | 63,009 |
| ENST00000429370.5 | hg19 | chr11 | 107,373,755 | 107,436,461 | 62,707 |
| ENST00000389568.7 | hg19 | chr11 | 107,375,321 | 107,436,244 | 60,924 |
| ENST00000417449.6 | hg19 | chr11 | 107,375,384 | 107,436,468 | 61,085 |
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