PQBP1 polyglutamine binding protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 30 |
Likely pathogenic | 0 | 26 |
Benign | 0 | 35 |
Likely benign | 0 | 70 |
Conflicting classifications of pathogenicity | 0 | 24 |
not provided | 6 | 0 |
Uncertain significance | 0 | 160 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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56 |
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245 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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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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Category | : |
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Search word | : | |
Filtering | : |
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 | MRX2 |
SYNONYM | MRX55 |
SYNONYM | MRXS3 |
SYNONYM | MRXS8 |
SYNONYM | NPW38 |
SYNONYM | RENS1 |
SYNONYM | SHS |
MIM | 300463 OMIM |
HGNC | HGNC:9330 HGNC |
Ensembl | ENSG00000102103 Ensembl |
AllianceGenome | HGNC:9330 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000218224.9 | hg38 | chrX | 48,897,938 | 48,903,142 | 5,205 |
ENST00000651767.1 | hg38 | chrX | 48,890,197 | 48,903,105 | 12,909 |
ENST00000376566.8 | hg38 | chrX | 48,897,912 | 48,903,142 | 5,231 |
ENST00000376563.6 | hg38 | chrX | 48,897,952 | 48,903,143 | 5,192 |
ENST00000247140.8 | hg38 | chrX | 48,897,940 | 48,903,142 | 5,203 |
ENST00000396763.6 | hg38 | chrX | 48,898,260 | 48,903,143 | 4,884 |
ENST00000443648.6 | hg38 | chrX | 48,898,041 | 48,903,143 | 5,103 |
ENST00000456306.2 | hg38 | chrX | 48,898,318 | 48,903,143 | 4,826 |
ENST00000447146.7 | hg38 | chrX | 48,897,930 | 48,903,143 | 5,214 |
ENST00000376566.8 | hg19 | chrX | 48,755,195 | 48,760,419 | 5,225 |
ENST00000651767.1 | hg19 | chrX | 48,747,480 | 48,760,382 | 12,903 |
ENST00000447146.7 | hg19 | chrX | 48,755,213 | 48,760,420 | 5,208 |
ENST00000218224.9 | hg19 | chrX | 48,755,221 | 48,760,419 | 5,199 |
ENST00000247140.8 | hg19 | chrX | 48,755,223 | 48,760,419 | 5,197 |
ENST00000376563.6 | hg19 | chrX | 48,755,235 | 48,760,420 | 5,186 |
ENST00000396763.6 | hg19 | chrX | 48,755,543 | 48,760,420 | 4,878 |
ENST00000443648.6 | hg19 | chrX | 48,755,324 | 48,760,420 | 5,097 |
ENST00000456306.2 | hg19 | chrX | 48,755,601 | 48,760,420 | 4,820 |
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