WNK3 WNK lysine deficient protein kinase 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 12 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 16 |
Likely benign | 0 | 42 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 144 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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200 |
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14 |
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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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 |
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SYNONYM | MRXS2 |
SYNONYM | PRKWNK3 |
SYNONYM | PRS |
MIM | 300358 OMIM |
HGNC | HGNC:14543 HGNC |
Ensembl | ENSG00000196632 Ensembl |
AllianceGenome | HGNC:14543 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000375169.7 | hg38 | chrX | 54,192,823 | 54,358,005 | 165,183 |
ENST00000354646.7 | hg38 | chrX | 54,192,823 | 54,358,046 | 165,224 |
ENST00000375169.7 | hg19 | chrX | 54,219,256 | 54,384,438 | 165,183 |
ENST00000354646.7 | hg19 | chrX | 54,219,256 | 54,384,479 | 165,224 |
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