TALDO1 transaldolase 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 16 |
Likely pathogenic | 0 | 14 |
Benign | 0 | 14 |
Likely benign | 0 | 162 |
Conflicting classifications of pathogenicity | 0 | 22 |
not provided | 0 | 2 |
Uncertain significance | 0 | 192 |
Ranking
ClinVar | |
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0 |
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0 |
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74 |
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308 |
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10 |
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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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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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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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 | TAL |
SYNONYM | TAL-H |
SYNONYM | TALDOR |
SYNONYM | TALH |
MIM | 602063 OMIM |
HGNC | HGNC:11559 HGNC |
Ensembl | ENSG00000177156 Ensembl |
AllianceGenome | HGNC:11559 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000528097.5 | hg38 | chr11 | 747,428 | 765,012 | 17,585 |
ENST00000319006.8 | hg38 | chr11 | 747,464 | 765,012 | 17,549 |
ENST00000528097.5 | hg19 | chr11 | 747,428 | 765,012 | 17,585 |
ENST00000319006.8 | hg19 | chr11 | 747,464 | 765,012 | 17,549 |
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