LIMK1 LIM domain kinase 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 26 |
Likely benign | 0 | 70 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 3 | 0 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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14 |
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130 |
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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
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 |
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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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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 | LIMK |
SYNONYM | LIMK-1 |
MIM | 601329 OMIM |
HGNC | HGNC:6613 HGNC |
Ensembl | ENSG00000106683 Ensembl |
AllianceGenome | HGNC:6613 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000418310.5 | hg38 | chr7 | 74,082,933 | 74,122,525 | 39,593 |
ENST00000336180.7 | hg38 | chr7 | 74,083,804 | 74,122,525 | 38,722 |
ENST00000538333.3 | hg38 | chr7 | 74,093,079 | 74,121,458 | 28,380 |
ENST00000418310.5 | hg19 | chr7 | 73,497,263 | 73,536,855 | 39,593 |
ENST00000336180.7 | hg19 | chr7 | 73,498,134 | 73,536,855 | 38,722 |
ENST00000538333.3 | hg19 | chr7 | 73,507,409 | 73,535,788 | 28,380 |
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