MTFR2 mitochondrial fission regulator 2
Information
- Symbol
- MTFR2
- Type
- protein-coding
- Description
- mitochondrial fission regulator 2
- Entrez Gene ID
- 113115
- Genome
- hg19
- Position
- chr6:136,552,172-136,571,449
- Genome
- hg38
- Position
- chr6:136,231,034-136,250,311
- HGNC
- HGNC:21115 HGNC
- Ensembl
- ENSG00000146410 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | DUFD1 |
SYNONYM | FAM54A |
HGNC | HGNC:21115 HGNC |
Ensembl | ENSG00000146410 Ensembl |
AllianceGenome | HGNC:21115 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000420702.6 | hg38 | chr6 | 136,231,034 | 136,250,311 | 19,278 |
ENST00000451457.6 | hg38 | chr6 | 136,231,024 | 136,250,324 | 19,301 |
ENST00000451457.6 | hg19 | chr6 | 136,552,162 | 136,571,462 | 19,301 |
ENST00000420702.6 | hg19 | chr6 | 136,552,172 | 136,571,449 | 19,278 |
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