ILK integrin linked kinase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 42 |
Likely benign | 0 | 340 |
Conflicting classifications of pathogenicity | 0 | 16 |
Uncertain significance | 0 | 400 |
Ranking
ClinVar | |
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0 |
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0 |
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198 |
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552 |
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10 |
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.]
Locus Zoom
Variants
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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 |
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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 | HEL-S-28 |
SYNONYM | ILK-1 |
SYNONYM | ILK-2 |
SYNONYM | P59 |
SYNONYM | p59ILK |
MIM | 602366 OMIM |
HGNC | HGNC:6040 HGNC |
Ensembl | ENSG00000166333 Ensembl |
AllianceGenome | HGNC:6040 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000528995.5 | hg38 | chr11 | 6,603,787 | 6,610,866 | 7,080 |
ENST00000396751.6 | hg38 | chr11 | 6,603,816 | 6,610,870 | 7,055 |
ENST00000420936.6 | hg38 | chr11 | 6,603,758 | 6,610,833 | 7,076 |
ENST00000532063.5 | hg38 | chr11 | 6,603,708 | 6,610,874 | 7,167 |
ENST00000627400.1 | hg38 | chr11 | 6,604,272 | 6,604,874 | 603 |
ENST00000299421.9 | hg38 | chr11 | 6,603,774 | 6,610,870 | 7,097 |
ENST00000537806.5 | hg38 | chr11 | 6,603,744 | 6,610,835 | 7,092 |
ENST00000532063.5 | hg19 | chr11 | 6,624,938 | 6,632,105 | 7,168 |
ENST00000537806.5 | hg19 | chr11 | 6,624,974 | 6,632,066 | 7,093 |
ENST00000420936.6 | hg19 | chr11 | 6,624,988 | 6,632,064 | 7,077 |
ENST00000299421.9 | hg19 | chr11 | 6,625,004 | 6,632,101 | 7,098 |
ENST00000528995.5 | hg19 | chr11 | 6,625,017 | 6,632,097 | 7,081 |
ENST00000396751.6 | hg19 | chr11 | 6,625,046 | 6,632,101 | 7,056 |
ENST00000627400.1 | hg19 | chr11 | 6,625,502 | 6,626,104 | 603 |
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