FKBP10 - Gene browser

FKBP10

FKBP prolyl isomerase 10

HCNC Approved Symbol: FKBP10 (HGNC:18169)
Genomic Coordinates: 17:41,813,004 - 41,823,213 (17q21.2)
Synonyms: hFKBP65, FKBP65, FLJ22041, FKBP6, FLJ20683, FLJ23833
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

11Patients

In total, 11 patients were diagnosed with a variant in the FKBP10 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

011
Patient count

Bone fractures: 4 (36.4%)
Patient Count: 4 (36.4%)
% of total patients presenting each phenotype is shown in parentheses.
4 (36.4%)
Bone fragility: 3 (27.3%)
Patient Count: 3 (27.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (27.3%)
Increased susceptibility to fractures: 3 (27.3%)
Patient Count: 3 (27.3%)
% of total patients presenting each phenotype is shown in parentheses.
3 (27.3%)
Bone fractures, multiple: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)
Abnormality of the ribs: 2 (18.2%)
Patient Count: 2 (18.2%)
% of total patients presenting each phenotype is shown in parentheses.
2 (18.2%)