TPRX1 tetrapeptide repeat homeobox 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 24 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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92 |
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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 |
---|---|
SYNONYM | TPRX |
MIM | 611166 OMIM |
HGNC | HGNC:32174 HGNC |
Ensembl | ENSG00000178928 Ensembl |
AllianceGenome | HGNC:32174 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000698655.1 | hg38 | chr19 | 47,801,232 | 47,804,551 | 3,320 |
ENST00000535759.2 | hg38 | chr19 | 47,801,775 | 47,819,051 | 17,277 |
ENST00000322175.8 | hg38 | chr19 | 47,801,562 | 47,804,551 | 2,990 |
ENST00000698655.1 | hg19 | chr19 | 48,304,489 | 48,307,808 | 3,320 |
ENST00000322175.8 | hg19 | chr19 | 48,304,819 | 48,307,808 | 2,990 |
ENST00000535759.2 | hg19 | chr19 | 48,305,032 | 48,322,308 | 17,277 |
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