Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
4831 to 4840 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

4831
FRAT regulator of Wnt signaling pathway 1
-
Diabetes mellitus type 2

4832
FRAT regulator of Wnt signaling pathway 2
FRAT-2
Cholecystolithiasis, Gallstones, Diabetes mellitus type 2

4833
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

4834
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

4835
FRAS1 related extracellular matrix 3
-
Major depressive disorder, Depression

4836
Frey regulator of sperm-oocyte fusion 1
C11orf94, Frey
Insomnia

4837
FSHD region gene 1
FRG1A, FSG1
Congenital pulmonary artery atresia, Facioscapulohumeral muscular dystrophy

4838
Fyn related Src family tyrosine kinase
GTK, PTK5, RAK
Glaucoma, Gout, Hemifacial microsomia

4839
FERM domain containing 1
bA164L23.1
Attention deficit hyperactivity disorder, Venous thromboembolism

4840
FERM domain containing 3
4.1O, EPB41L4O, EPB41LO, P410
Chloracne, Dementia, Hypertension, Lewy body disease, Sarcoidosis, Upper aerodigestive tract neoplasm