TAOK2 TAO kinase 2
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 46 |
| Likely benign | 0 | 560 |
| not provided | 10 | 0 |
| Uncertain significance | 0 | 726 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
102 |
 |
1,224 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | MAP3K17 |
| SYNONYM | PSK |
| SYNONYM | PSK1 |
| SYNONYM | PSK1-BETA |
| SYNONYM | TAO1 |
| SYNONYM | TAO2 |
| SYNONYM | Tao2beta |
| MIM | 613199 OMIM |
| HGNC | HGNC:16835 HGNC |
| Ensembl | ENSG00000149930 Ensembl |
| AllianceGenome | HGNC:16835 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000279394.7 | hg38 | chr16 | 29,974,281 | 29,992,261 | 17,981 |
| ENST00000543033.5 | hg38 | chr16 | 29,974,182 | 29,988,181 | 14,000 |
| ENST00000416441.2 | hg38 | chr16 | 29,980,352 | 29,988,398 | 8,047 |
| ENST00000308893.9 | hg38 | chr16 | 29,973,868 | 29,988,393 | 14,526 |
| ENST00000308893.9 | hg19 | chr16 | 29,985,189 | 29,999,714 | 14,526 |
| ENST00000543033.5 | hg19 | chr16 | 29,985,503 | 29,999,502 | 14,000 |
| ENST00000279394.7 | hg19 | chr16 | 29,985,602 | 30,003,582 | 17,981 |
| ENST00000416441.2 | hg19 | chr16 | 29,991,673 | 29,999,719 | 8,047 |
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