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"
491 to 500 of 584 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

491
Formyl peptide receptor 2
ALX, ALXR, FMLP-R-II, FMLPX, FPR2A, FPRH1, FPRH2, FPRL1, HM63, LXA4R
Crohn disease

492
Formyl peptide receptor 3
FML2_HUMAN, FMLP-R-II, FMLPY, FPRH1, FPRH2, FPRL2, RMLP-R-I
Asthma, Respiratory system disease, Tourette syndrome

493
FRA10A associated CGG repeat 1
C10orf4, F26C11.1-like, FRA10A, NEDGFC
Neurodevelopmental disorder

494
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

495
FRAT regulator of Wnt signaling pathway 1
-
Diabetes mellitus type 2

496
FRAT regulator of Wnt signaling pathway 2
FRAT-2
Cholecystolithiasis, Gallstones, Diabetes mellitus type 2

497
FRAS1 related extracellular matrix 1
BNAR, C9orf143, C9orf145, C9orf154, MOTA, TILRR, TRIGNO2
Bifid nose, Bnar syndrome, Congenital anomalies of the kidney and urinary tract, Cardiovascular disease, Kidney disease, Lymphocytic leukemia, Congenital diaphragmatic hernia, Craniosynostosis, Eye abnormalities, Craniofaciosynostosis, Metabolic syndrome, Willis-ekbom disease, Trigonocephaly, Diabetes mellitus type 2

498
FRAS1 related extracellular matrix 2
CRYPTOP, FRASRS2
Ambiguous genitalia, Congenital anomalies of the kidney and urinary tract, Cryptophthalmia, Congenital diaphragmatic hernia, Cryptophthalmos syndrome, Cryptotria, Epidermolysis bullosa, Fraser syndrome, Psoriasis, Schizophrenia, Syndactyly

499
FRAS1 related extracellular matrix 3
-
Major depressive disorder, Depression

500
Frey regulator of sperm-oocyte fusion 1
C11orf94, Frey
Insomnia