MTIF2 mitochondrial translational initiation factor 2
Information
- Symbol
- MTIF2
- Type
- protein-coding
- Description
- mitochondrial translational initiation factor 2
- Entrez Gene ID
- 4528
- Genome
- hg19
- Position
- chr2:55,463,731-55,496,367
- Genome
- hg38
- Position
- chr2:55,236,595-55,269,231
- MIM
- 603766 OMIM
- HGNC
- HGNC:7441 HGNC
- Ensembl
- ENSG00000085760 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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88 |
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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 |
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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000263629.9 | hg38 | chr2 | 55,236,595 | 55,269,231 | 32,637 |
ENST00000394600.7 | hg38 | chr2 | 55,236,621 | 55,263,868 | 27,248 |
ENST00000403721.5 | hg38 | chr2 | 55,236,595 | 55,269,243 | 32,649 |
ENST00000263629.9 | hg19 | chr2 | 55,463,731 | 55,496,367 | 32,637 |
ENST00000403721.5 | hg19 | chr2 | 55,463,731 | 55,496,379 | 32,649 |
ENST00000394600.7 | hg19 | chr2 | 55,463,757 | 55,491,004 | 27,248 |
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