DEXI Dexi homolog
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | MYLE |
MIM | 617901 OMIM |
HGNC | HGNC:13267 HGNC |
Ensembl | ENSG00000182108 Ensembl |
AllianceGenome | HGNC:13267 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000331808.5 | hg38 | chr16 | 10,928,891 | 10,942,468 | 13,578 |
ENST00000469379.5 | hg38 | chr16 | 10,928,891 | 10,942,131 | 13,241 |
ENST00000570440.2 | hg38 | chr16 | 10,936,607 | 10,942,460 | 5,854 |
ENST00000469379.5 | hg19 | chr16 | 11,022,748 | 11,035,988 | 13,241 |
ENST00000331808.5 | hg19 | chr16 | 11,022,748 | 11,036,325 | 13,578 |
ENST00000570440.2 | hg19 | chr16 | 11,030,464 | 11,036,317 | 5,854 |
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