MIOS meiosis regulator for oocyte development
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 72 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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82 |
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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
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 |
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 | MIO |
SYNONYM | Sea4 |
SYNONYM | Yulink |
MIM | 615359 OMIM |
HGNC | HGNC:21905 HGNC |
Ensembl | ENSG00000164654 Ensembl |
AllianceGenome | HGNC:21905 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000340080.9 | hg38 | chr7 | 7,566,884 | 7,608,932 | 42,049 |
ENST00000405785.5 | hg38 | chr7 | 7,566,875 | 7,607,223 | 40,349 |
ENST00000405785.5 | hg19 | chr7 | 7,606,506 | 7,646,854 | 40,349 |
ENST00000340080.9 | hg19 | chr7 | 7,606,515 | 7,648,563 | 42,049 |
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