MRS2 magnesium transporter MRS2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 4 | 0 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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38 |
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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
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 |
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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 |
Type | ID |
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SYNONYM | HPT |
SYNONYM | MRS2L |
MIM | 619307 OMIM |
HGNC | HGNC:13785 HGNC |
Ensembl | ENSG00000124532 Ensembl |
AllianceGenome | HGNC:13785 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000378386.8 | hg38 | chr6 | 24,402,936 | 24,426,190 | 23,255 |
ENST00000378353.5 | hg38 | chr6 | 24,402,954 | 24,423,476 | 20,523 |
ENST00000274747.11 | hg38 | chr6 | 24,402,908 | 24,426,194 | 23,287 |
ENST00000443868.6 | hg38 | chr6 | 24,402,908 | 24,426,194 | 23,287 |
ENST00000274747.11 | hg19 | chr6 | 24,403,136 | 24,426,422 | 23,287 |
ENST00000443868.6 | hg19 | chr6 | 24,403,136 | 24,426,422 | 23,287 |
ENST00000378386.8 | hg19 | chr6 | 24,403,164 | 24,426,418 | 23,255 |
ENST00000378353.5 | hg19 | chr6 | 24,403,182 | 24,423,704 | 20,523 |
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