KLF4 KLF transcription factor 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 14 |
Likely benign | 0 | 26 |
not provided | 8 | 0 |
Uncertain significance | 0 | 56 |
Ranking
ClinVar | |
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0 |
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0 |
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12 |
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78 |
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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
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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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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | EZF |
SYNONYM | GKLF |
MIM | 602253 OMIM |
HGNC | HGNC:6348 HGNC |
Ensembl | ENSG00000136826 Ensembl |
AllianceGenome | HGNC:6348 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000374672.5 | hg38 | chr9 | 107,484,852 | 107,489,769 | 4,918 |
ENST00000610832.1 | hg38 | chr9 | 107,484,854 | 107,489,766 | 4,913 |
ENST00000374672.5 | hg19 | chr9 | 110,247,133 | 110,252,050 | 4,918 |
ENST00000610832.1 | hg19 | chr9 | 110,247,135 | 110,252,047 | 4,913 |
Key | Value |
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strand | - |
start | 110,247,132 |
Vogelstein | OG |
Gene Symbol | KLF4 |
Entrez GeneId | 9,314 |
Chr Band | 9q31 |
end | 110,252,000 |
chr | chr9 |
Name | Kruppel-like factor 4 |
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