Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4721 to 4730 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4721
Factor interacting with PAPOLA and CPSF1
FIP1, Rhe, hFip1
Eosinophilic leukemia, Congestive heart failure, Eosinophilia, Heart failure, Hypereosinophilic syndrome

4722
FIGNL1 interacting regulator of recombination and mitosis
Apolo1, C1orf112, FLIP, MEICA1
Amyotrophic lateral sclerosis, Diabetes mellitus type 2, Venous thromboembolism

4723
Fission, mitochondrial 1
CGI-135, TTC11
Neuronal ceroid lipofuscinosis, Ventricular remodeling

4724
Fat storage inducing transmembrane protein 2
C20orf142, Fit2, SIDDIS, dJ881L22.2
Diabetes mellitus type 2

4725
FLT3 interacting zinc finger 1
ZNF798
Periodontitis

4726
Four-jointed box kinase 1
-
Brain neoplasms

4727
FKBP prolyl isomerase 10
BRKS, BRKS1, FKBP65, OI11, OI6, PPIASE, TLH1, hFKBP65
Arthrogryposis, Bone fragility with contractures, arterial rupture, and deafness, Bruck syndrome, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

4728
FKBP prolyl isomerase 14
EDSKMH, EDSKSCL2, FKBP22, IPBP12
Congenital contractural arachnodactyly, Congenital muscular dystrophy, Desbuquois syndrome, Ehlers-danlos syndrome

4729
FKBP prolyl isomerase family member 15
FKBP133, KIAA0674, PPP1R76
Amphetamine or sympathomimetic abuse

4730
FKBP prolyl isomerase 1A
FKBP-12, FKBP-1A, FKBP1, FKBP12, PKC12, PKCI2, PPIASE
Esophageal squamous cell carcinoma, Hearing loss, Liver cirrhosis, Metabolic syndrome, Sjogren syndrome, Diabetes mellitus type 2