MMGT1 membrane magnesium transporter 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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20 |
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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 |
Search Word
Target data | : |
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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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 |
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SYNONYM | EMC5 |
SYNONYM | TMEM32 |
MIM | 301098 OMIM |
HGNC | HGNC:28100 HGNC |
Ensembl | ENSG00000169446 Ensembl |
AllianceGenome | HGNC:28100 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000679621.1 | hg38 | chrX | 135,964,678 | 135,974,029 | 9,352 |
ENST00000680510.2 | hg38 | chrX | 135,962,152 | 135,974,013 | 11,862 |
ENST00000305963.3 | hg38 | chrX | 135,960,588 | 135,973,988 | 13,401 |
ENST00000681201.1 | hg38 | chrX | 135,963,173 | 135,973,684 | 10,512 |
ENST00000305963.3 | hg19 | chrX | 135,042,747 | 135,056,147 | 13,401 |
ENST00000680510.2 | hg19 | chrX | 135,044,311 | 135,056,172 | 11,862 |
ENST00000681201.1 | hg19 | chrX | 135,045,332 | 135,055,843 | 10,512 |
ENST00000679621.1 | hg19 | chrX | 135,046,837 | 135,056,188 | 9,352 |
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