FKBP8 FKBP prolyl isomerase 8
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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46 |
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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
[No Data.]
Locus Zoom
Variants
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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 | FKBP38 |
SYNONYM | FKBPr38 |
MIM | 604840 OMIM |
HGNC | HGNC:3724 HGNC |
Ensembl | ENSG00000105701 Ensembl |
AllianceGenome | HGNC:3724 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000608443.6 | hg38 | chr19 | 18,531,763 | 18,543,573 | 11,811 |
ENST00000596558.6 | hg38 | chr19 | 18,531,762 | 18,542,972 | 11,211 |
ENST00000597960.7 | hg38 | chr19 | 18,531,751 | 18,543,577 | 11,827 |
ENST00000222308.8 | hg38 | chr19 | 18,531,762 | 18,543,524 | 11,763 |
ENST00000597960.7 | hg19 | chr19 | 18,642,561 | 18,654,387 | 11,827 |
ENST00000596558.6 | hg19 | chr19 | 18,642,572 | 18,653,782 | 11,211 |
ENST00000222308.8 | hg19 | chr19 | 18,642,572 | 18,654,334 | 11,763 |
ENST00000608443.6 | hg19 | chr19 | 18,642,573 | 18,654,383 | 11,811 |
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