PTK6 protein tyrosine kinase 6
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 86 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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88 |
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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
[No Data.]
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Variants
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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 |
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | BRK |
MIM | 602004 OMIM |
HGNC | HGNC:9617 HGNC |
Ensembl | ENSG00000101213 Ensembl |
AllianceGenome | HGNC:9617 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000217185.3 | hg38 | chr20 | 63,528,425 | 63,537,370 | 8,946 |
ENST00000542869.3 | hg38 | chr20 | 63,528,001 | 63,537,376 | 9,376 |
ENST00000542869.3 | hg19 | chr20 | 62,159,354 | 62,168,729 | 9,376 |
ENST00000217185.3 | hg19 | chr20 | 62,159,778 | 62,168,723 | 8,946 |
Key | Value |
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strand | - |
start | 62,159,775 |
Gene Symbol | PTK6 |
Entrez GeneId | 5,753 |
Chr Band | 20q13.3 |
end | 62,168,722 |
chr | chr20 |
Name | protein tyrosine kinase 6 |
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