MTX1 metaxin 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 1 |
Uncertain significance | 0 | 30 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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31 |
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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
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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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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 |
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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 |
Type | ID |
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SYNONYM | MTX |
SYNONYM | MTXN |
MIM | 600605 OMIM |
HGNC | HGNC:7504 HGNC |
Ensembl | ENSG00000173171 Ensembl |
AllianceGenome | HGNC:7504 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000609421.1 | hg38 | chr1 | 155,209,247 | 155,213,824 | 4,578 |
ENST00000368376.8 | hg38 | chr1 | 155,208,695 | 155,213,823 | 5,129 |
ENST00000316721.8 | hg38 | chr1 | 155,208,797 | 155,213,823 | 5,027 |
ENST00000368376.8 | hg19 | chr1 | 155,178,486 | 155,183,614 | 5,129 |
ENST00000316721.8 | hg19 | chr1 | 155,178,588 | 155,183,614 | 5,027 |
ENST00000609421.1 | hg19 | chr1 | 155,179,038 | 155,183,615 | 4,578 |
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