MDFI MyoD family inhibitor
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 28 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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32 |
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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
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | I-MF |
| SYNONYM | I-mfa |
| MIM | 604971 OMIM |
| HGNC | HGNC:6967 HGNC |
| Ensembl | ENSG00000112559 Ensembl |
| AllianceGenome | HGNC:6967 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000373051.6 | hg38 | chr6 | 41,637,068 | 41,654,239 | 17,172 |
| ENST00000373050.8 | hg38 | chr6 | 41,638,477 | 41,653,639 | 15,163 |
| ENST00000230321.11 | hg38 | chr6 | 41,638,468 | 41,654,244 | 15,777 |
| ENST00000373051.6 | hg19 | chr6 | 41,604,806 | 41,621,977 | 17,172 |
| ENST00000230321.11 | hg19 | chr6 | 41,606,206 | 41,621,982 | 15,777 |
| ENST00000373050.8 | hg19 | chr6 | 41,606,215 | 41,621,377 | 15,163 |
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