Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4571 to 4580 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4571
F-box and leucine rich repeat protein 4
FBL4, FBL5, MTDPS13
Mitochondrial dna depletion syndrome, Global developmental delay, Insomnia, Leigh syndrome, Major depressive disorder, Mitochondrial disease, Mitochondrial encephalomyopathy, Moyamoya angiopathy

4572
F-box and leucine rich repeat protein 7
FBL6, FBL7
Alzheimer disease, Asthma, Kidney disease, Color vision deficiency, Digeorge syndrome, Hemorrhoid, Kidney failure, Lung cancer, Obesity, Oligodendroglioma, Scoliosis, Squamous cell carcinoma

4573
F-box and leucine rich repeat protein 8
FBL8
Congenital lamellar cataract

4574
F-box protein 11
FBX11, IDDFBA, PRMT9, UBR6, UG063H01, VIT1
Alzheimer disease, Asthma, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Bipolar disorder, Lynch syndrome, Developmental disability, Diverticular disease, Insomnia, Intellectual developmental disorder dysmorphic behavioral, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability
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4575
F-box protein 15
FBX15
Tourette syndrome, Insomnia, Oligodendroglioma, Smooth surface dental caries, Venous thromboembolism

4576
F-box protein 17
FBG4, FBX26, FBXO26, Fbx17
Synovitis, acne, pustulosis, hyperostosis, and osteitis

4577
F-box protein 21
FBX21
Astrocytoma, Central nervous system cancer, Coronary artery disease, Glioblastoma, Glioma, Insomnia, Metabolic syndrome, Diabetes mellitus type 2

4578
F-box protein 22
FBX22, FISTC1, TYMAS
Gout, Neurodevelopmental disorder

4579
F-box protein 25
FBX25
Osteonecrosis of the femoral head, Moyamoya disease

4580
F-box protein 27
FBG5, Fbx27
Iga nephropathy