TXNL4B thioredoxin like 4B
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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
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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 | |||||
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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 | DLP |
SYNONYM | Dim2 |
MIM | 617722 OMIM |
HGNC | HGNC:26041 HGNC |
Ensembl | ENSG00000140830 Ensembl |
AllianceGenome | HGNC:26041 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000423037.5 | hg38 | chr16 | 72,084,859 | 72,093,869 | 9,011 |
ENST00000268483.8 | hg38 | chr16 | 72,084,857 | 72,093,620 | 8,764 |
ENST00000426362.6 | hg38 | chr16 | 72,086,397 | 72,094,431 | 8,035 |
ENST00000268483.8 | hg19 | chr16 | 72,118,756 | 72,127,519 | 8,764 |
ENST00000423037.5 | hg19 | chr16 | 72,118,758 | 72,127,768 | 9,011 |
ENST00000426362.6 | hg19 | chr16 | 72,120,296 | 72,128,330 | 8,035 |
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