Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4821 to 4830 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4821
Forkhead box R1
DLNB13, FOXN5
Astrocytoma

4822
FAD dependent oxidoreductase domain containing 1
FP634, H17, MC1DN19
Developmental delay, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy

4823
Folylpolyglutamate synthase
-
Rheumatoid arthritis, Colorectal neoplasms

4824
Fucose-1-phosphate guanylyltransferase
GFPP
Renal cell carcinoma

4825
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

4826
Formyl peptide receptor 1
FMLP, FPR
Cervical cancer, Obstructive pulmonary disease, Tourette syndrome, Gingival diseases, Multiple sclerosis, Periodontitis, Respiratory system disease

4827
Formyl peptide receptor 2
ALX, ALXR, FMLP-R-II, FMLPX, FPR2A, FPRH1, FPRH2, FPRL1, HM63, LXA4R
Crohn disease

4828
Formyl peptide receptor 3
FML2_HUMAN, FMLP-R-II, FMLPY, FPRH1, FPRH2, FPRL2, RMLP-R-I
Asthma, Respiratory system disease, Tourette syndrome

4829
FRA10A associated CGG repeat 1
C10orf4, F26C11.1-like, FRA10A, NEDGFC
Neurodevelopmental disorder

4830
Fraser extracellular matrix complex subunit 1
FRASRS1
Alzheimer disease, Congenital anomalies of the kidney and urinary tract, Obstructive pulmonary disease, Renal agenesis, Congenital diaphragmatic hernia, Congenital left-sided heart lesions, Cryptophthalmos syndrome, Fraser syndrome, Generalized anxiety disorder, Retinal detachment