VCPKMT valosin containing protein lysine methyltransferase
Information
- Symbol
- VCPKMT
- Type
- protein-coding
- Description
- valosin containing protein lysine methyltransferase
- Entrez Gene ID
- 79609
- Genome
- hg19
- Position
- chr14:50,575,355-50,583,290
- Genome
- hg38
- Position
- chr14:50,108,637-50,116,572
- MIM
- 615260 OMIM
- HGNC
- HGNC:20352 HGNC
- Ensembl
- ENSG00000100483 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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36 |
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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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MGeND data only
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| 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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| 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 | C14orf138 |
| SYNONYM | METTL21D |
| SYNONYM | VCP-KMT |
| MIM | 615260 OMIM |
| HGNC | HGNC:20352 HGNC |
| Ensembl | ENSG00000100483 Ensembl |
| AllianceGenome | HGNC:20352 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000395860.7 | hg38 | chr14 | 50,108,637 | 50,116,572 | 7,936 |
| ENST00000395859.2 | hg38 | chr14 | 50,109,537 | 50,116,600 | 7,064 |
| ENST00000395860.7 | hg19 | chr14 | 50,575,355 | 50,583,290 | 7,936 |
| ENST00000395859.2 | hg19 | chr14 | 50,576,255 | 50,583,318 | 7,064 |
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