MNT MAX network transcriptional repressor
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
not provided | 1 | 0 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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42 |
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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 | : | |
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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 |
---|---|
SYNONYM | MAD6 |
SYNONYM | MXD6 |
SYNONYM | ROX |
SYNONYM | bHLHd3 |
SYNONYM | lncRNA-HAL |
MIM | 603039 OMIM |
HGNC | HGNC:7188 HGNC |
Ensembl | ENSG00000070444 Ensembl |
AllianceGenome | HGNC:7188 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000575394.1 | hg38 | chr17 | 2,387,909 | 2,401,104 | 13,196 |
ENST00000174618.5 | hg38 | chr17 | 2,384,073 | 2,401,060 | 16,988 |
ENST00000174618.5 | hg19 | chr17 | 2,287,367 | 2,304,354 | 16,988 |
ENST00000575394.1 | hg19 | chr17 | 2,291,203 | 2,304,398 | 13,196 |
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