MAJIN membrane anchored junction protein
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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6 |
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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 |
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 | C11orf85 |
MIM | 617130 OMIM |
HGNC | HGNC:27441 HGNC |
Ensembl | ENSG00000168070 Ensembl |
AllianceGenome | HGNC:27441 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000301896.6 | hg38 | chr11 | 64,938,230 | 64,972,108 | 33,879 |
ENST00000432175.5 | hg38 | chr11 | 64,938,454 | 64,960,137 | 21,684 |
ENST00000530444.5 | hg38 | chr11 | 64,938,230 | 64,972,023 | 33,794 |
ENST00000530444.5 | hg19 | chr11 | 64,705,702 | 64,739,495 | 33,794 |
ENST00000301896.6 | hg19 | chr11 | 64,705,702 | 64,739,580 | 33,879 |
ENST00000432175.5 | hg19 | chr11 | 64,705,926 | 64,727,609 | 21,684 |
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