FKBP4 FKBP prolyl isomerase 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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54 |
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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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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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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 | FKBP51 |
SYNONYM | FKBP52 |
SYNONYM | FKBP59 |
SYNONYM | HBI |
SYNONYM | Hsp56 |
SYNONYM | PPIase |
SYNONYM | p52 |
MIM | 600611 OMIM |
HGNC | HGNC:3720 HGNC |
Ensembl | ENSG00000004478 Ensembl |
AllianceGenome | HGNC:3720 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000630279.1 | hg38 | chr12 | 2,795,140 | 2,796,315 | 1,176 |
ENST00000001008.6 | hg38 | chr12 | 2,794,970 | 2,805,423 | 10,454 |
ENST00000001008.6 | hg19 | chr12 | 2,904,136 | 2,914,589 | 10,454 |
ENST00000630279.1 | hg19 | chr12 | 2,904,306 | 2,905,481 | 1,176 |
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