Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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4851 to 4860 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4851
FRA10A associated CGG repeat 1
C10orf4, F26C11.1-like, FRA10A, NEDGFC
Neurodevelopmental disorder

4852
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

4853
FRAT regulator of Wnt signaling pathway 1
-
Diabetes mellitus type 2

4854
FRAT regulator of Wnt signaling pathway 2
FRAT-2
Cholecystolithiasis, Gallstones, Diabetes mellitus type 2

4855
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

4856
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

4857
FRAS1 related extracellular matrix 3
-
Major depressive disorder, Depression

4858
Frey regulator of sperm-oocyte fusion 1
C11orf94, Frey
Insomnia

4859
FSHD region gene 1
FRG1A, FSG1
Congenital pulmonary artery atresia, Facioscapulohumeral muscular dystrophy

4860
Fyn related Src family tyrosine kinase
GTK, PTK5, RAK
Glaucoma, Gout, Hemifacial microsomia