TTK TTK protein kinase
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 6 |
| Likely benign | 0 | 8 |
| not provided | 18 | 0 |
| Uncertain significance | 0 | 70 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
84 |
![]() |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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 | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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 | CT96 |
| SYNONYM | ESK |
| SYNONYM | MPH1 |
| SYNONYM | MPS1 |
| SYNONYM | MPS1L1 |
| SYNONYM | PYT |
| MIM | 604092 OMIM |
| HGNC | HGNC:12401 HGNC |
| Ensembl | ENSG00000112742 Ensembl |
| AllianceGenome | HGNC:12401 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000627129.1 | hg38 | chr6 | 80,005,844 | 80,007,838 | 1,995 |
| ENST00000230510.7 | hg38 | chr6 | 80,004,147 | 80,042,527 | 38,381 |
| ENST00000509894.5 | hg38 | chr6 | 80,003,887 | 80,042,527 | 38,641 |
| ENST00000369798.7 | hg38 | chr6 | 80,004,649 | 80,042,527 | 37,879 |
| ENST00000509894.5 | hg19 | chr6 | 80,713,604 | 80,752,244 | 38,641 |
| ENST00000230510.7 | hg19 | chr6 | 80,713,864 | 80,752,244 | 38,381 |
| ENST00000369798.7 | hg19 | chr6 | 80,714,366 | 80,752,244 | 37,879 |
| ENST00000627129.1 | hg19 | chr6 | 80,715,561 | 80,717,555 | 1,995 |
Genome browser




