Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4711 to 4720 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4711
FKBP prolyl isomerase 2
FKBP-13, FKBP13, PPIase
Bipolar disorder, Metabolic syndrome, Stomach neoplasms, Diabetes mellitus type 2

4712
FKBP prolyl isomerase 3
FKBP-25, FKBP-3, FKBP25, PPIase
Hypertensive nephropathy

4713
FKBP prolyl isomerase 4
FKBP51, FKBP52, FKBP59, HBI, Hsp56, PPIase, p52
Hypogonadism, Major depressive disorder, Testicular disease, Depression

4714
FKBP prolyl isomerase 5
AIG6, FKBP51, FKBP54, P54, PPIase, Ptg-10
Rheumatoid arthritis, Asthma, Bipolar disorder, Depression, Colorectal adenoma, Colorectal cancer, Coronary artery disease, Major depressive disorder, Endometriosis, Hypothyroidism, Idiopathic pulmonary fibrosis, Mood disorder, Non-organic psychosis, Osteoarthritis, Psychotic disorders
View all (2 more)

4715
FKBP prolyl isomerase family member 6 (inactive)
FKBP36, SPGF77
Hyperlipidemia, Male infertility, Spermatogenic failure, Williams syndrome

4716
FKBP prolyl isomerase 8
FKBP38, FKBPr38
Alzheimer disease, Attention deficit hyperactivity disorder, Breast cancer, Crohn disease, Gastroesophageal reflux disease, Inflammatory bowel disease, Substance abuse

4717
FKBP prolyl isomerase 9
FKBP60, FKBP63, PPIase
Schizophrenia

4718
FKBP prolyl isomerase like
DIR1, NG7, WISP39
Alzheimer disease, Breast neoplasms, Interstitial cystitis, Hypothyroidism, Inflammatory bowel disease, Membranous glomerulonephritis, Nephrolithiasis, Psoriasis, Rheumatoid arthritis, Systemic lupus erythematosus

4719
Fukutin related protein
FKTR, LGMD2I, LGMDR9, MDC1C, MDDGA5, MDDGB5, MDDGC5
Limb girdle muscular dystrophy, Dilated cardiomyopathy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital myopathy, Limb-girdle muscular dystrophy, Muscle eye brain disease, Muscular dystrophy, Myopathy, Distal hereditary motor neuropathy, Paresthesia, Diabetes mellitus type 1, Diabetes mellitus type 2, Walker-warburg syndrome

4720
Fukutin
CMD1X, FCMD, LGMD2M, LGMDR13, MDDGA4, MDDGB4, MDDGC4
Limb girdle muscular dystrophy, Dilated cardiomyopathy, Cataract, Congenital muscular dystrophy, Global developmental delay, Muscle eye brain disease, Muscular dystrophy, Myocardial infarction, Walker-warburg syndrome