METTL15 methyltransferase 15, mitochondrial 12S rRNA N4-cytidine
Information
- Symbol
- METTL15
- Type
- protein-coding
- Description
- methyltransferase 15, mitochondrial 12S rRNA N4-cytidine
- Entrez Gene ID
- 196074
- Genome
- hg19
- Position
- chr11:28,129,935-28,355,054
- Genome
- hg38
- Position
- chr11:28,108,388-28,333,507
- MIM
- 618711 OMIM
- HGNC
- HGNC:26606 HGNC
- Ensembl
- ENSG00000169519 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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56 |
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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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Category | : |
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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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Filtering | : |
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 |
---|---|
SYNONYM | METT5D1 |
MIM | 618711 OMIM |
HGNC | HGNC:26606 HGNC |
Ensembl | ENSG00000169519 Ensembl |
AllianceGenome | HGNC:26606 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000634721.1 | hg38 | chr11 | 28,110,315 | 28,164,136 | 53,822 |
ENST00000406787.7 | hg38 | chr11 | 28,108,248 | 28,333,507 | 225,260 |
ENST00000303459.10 | hg38 | chr11 | 28,110,312 | 28,333,507 | 223,196 |
ENST00000634762.1 | hg38 | chr11 | 28,110,315 | 28,145,747 | 35,433 |
ENST00000407364.8 | hg38 | chr11 | 28,108,388 | 28,333,507 | 225,120 |
ENST00000403099.5 | hg38 | chr11 | 28,108,320 | 28,125,587 | 17,268 |
ENST00000406787.7 | hg19 | chr11 | 28,129,795 | 28,355,054 | 225,260 |
ENST00000403099.5 | hg19 | chr11 | 28,129,867 | 28,147,134 | 17,268 |
ENST00000407364.8 | hg19 | chr11 | 28,129,935 | 28,355,054 | 225,120 |
ENST00000303459.10 | hg19 | chr11 | 28,131,859 | 28,355,054 | 223,196 |
ENST00000634762.1 | hg19 | chr11 | 28,131,862 | 28,167,294 | 35,433 |
ENST00000634721.1 | hg19 | chr11 | 28,131,862 | 28,185,683 | 53,822 |
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