Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "F"
481 to 490 of 580 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
Forkhead box Q1
HFH1
Bipolar disorder, Breast cancer, Breast neoplasms, Colorectal cancer, Melanoma, Major depressive disorder, Scoliosis

482
Forkhead box R1
DLNB13, FOXN5
Astrocytoma

483
FAD dependent oxidoreductase domain containing 1
FP634, H17, MC1DN19
Developmental delay, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy

484
Folylpolyglutamate synthase
-
Rheumatoid arthritis, Colorectal neoplasms

485
Fucose-1-phosphate guanylyltransferase
GFPP
Renal cell carcinoma

486
FPGT-TNNI3K readthrough
CARK, TNNI3K
Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Attention deficit hyperactivity disorder, Bronchial disease, Cardiac conduction disease, Dilated cardiomyopathy, Central nervous system cancer, Glioblastoma, Glioma, Insomnia, Meniere disease, Metabolic syndrome, Obesity, Substance abuse, Diabetes mellitus type 2

487
Formyl peptide receptor 1
FMLP, FPR
Cervical cancer, Obstructive pulmonary disease, Tourette syndrome, Gingival diseases, Multiple sclerosis, Periodontitis, Respiratory system disease

488
Formyl peptide receptor 2
ALX, ALXR, FMLP-R-II, FMLPX, FPR2A, FPRH1, FPRH2, FPRL1, HM63, LXA4R
Crohn disease

489
Formyl peptide receptor 3
FML2_HUMAN, FMLP-R-II, FMLPY, FPRH1, FPRH2, FPRL2, RMLP-R-I
Asthma, Respiratory system disease, Tourette syndrome

490
FRA10A associated CGG repeat 1
C10orf4, F26C11.1-like, FRA10A, NEDGFC
Neurodevelopmental disorder