METTL2B methyltransferase 2B, tRNA N3-cytidine
Information
- Symbol
- METTL2B
- Type
- protein-coding
- Description
- methyltransferase 2B, tRNA N3-cytidine
- Entrez Gene ID
- 55798
- Genome
- hg19
- Position
- chr7:128,116,802-128,146,656
- Genome
- hg38
- Position
- chr7:128,476,748-128,506,602
- MIM
- 607846 OMIM
- HGNC
- HGNC:18272 HGNC
- Ensembl
- ENSG00000165055 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 38 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | METL |
| SYNONYM | METTL2 |
| SYNONYM | METTL2A |
| SYNONYM | PSENIP1 |
| MIM | 607846 OMIM |
| HGNC | HGNC:18272 HGNC |
| Ensembl | ENSG00000165055 Ensembl |
| AllianceGenome | HGNC:18272 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000480046.5 | hg38 | chr7 | 128,476,754 | 128,506,602 | 29,849 |
| ENST00000262432.13 | hg38 | chr7 | 128,476,748 | 128,506,602 | 29,855 |
| ENST00000262432.13 | hg19 | chr7 | 128,116,802 | 128,146,656 | 29,855 |
| ENST00000480046.5 | hg19 | chr7 | 128,116,808 | 128,146,656 | 29,849 |
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