FKBP14 Chromosome 7

FKBP prolyl isomerase 14
22 variants 22 Health Risk

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What This Gene Does
The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene. [provided by RefSeq, Mar 2012]
Gene Info
Gene Group
"EF-hand domain containing|FKBP prolyl isomerase family"
Locus Type
gene with protein product
Location
7p14.3
Ensembl
ENSG00000106080
Associated Conditions (11)
Ehlers-Danlos syndrome
kyphoscoliotic type
2
Cardiovascular phenotype
FKBP14-related disorder
Cervical cancer
Congenital muscular dystrophy
Pes valgus
Hypotonia
Thoracolumbar scoliosis
Joint hypermobility
Key Variants
All Variants (22)
RSID Category Clinical Significance Conditions
RS542254849 Health Risk Conflicting classifications of pathogenicity Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS747381671 Health Risk Conflicting classifications of pathogenicity Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS753775062 Health Risk Conflicting classifications of pathogenicity Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS757164371 Health Risk Conflicting classifications of pathogenicity Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS762279651 Health Risk Conflicting classifications of pathogenicity Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS763069544 Health Risk Conflicting classifications of pathogenicity Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS763168158 Health Risk Conflicting classifications of pathogenicity Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS1583734485 Health Risk Likely pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS747353360 Health Risk Likely pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS758622304 Health Risk Likely pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS775594340 Health Risk Likely pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS1430849353 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS1562840744 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS1583725395 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS1583738732 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS1790069483 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS2127949580 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS2127950876 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS770271683 Health Risk Pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS542489955 Health Risk Pathogenic/Likely pathogenic Congenital muscular dystrophy, Pes valgus, Hypotonia
RS753355121 Health Risk Pathogenic/Likely pathogenic Ehlers-Danlos syndrome, kyphoscoliotic type, 2
RS778176957 Health Risk Pathogenic/Likely pathogenic Cardiovascular phenotype, Ehlers-Danlos syndrome, kyphoscoliotic type
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