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
4691 to 4700 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

4691
Fibroblast growth factor receptor 3
ACH, CD333, CEK2, HSFGFR3EX, JTK4
Achondroplasia, Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Bladder cancer, Brachycephaly, Camptodactyly, tall stature, and hearing loss syndrome, Transitional cell carcinoma, Cataract, Catshl syndrome, Cervical cancer, Obstructive pulmonary disease, Cleft lip, Cleft palate, Colorectal cancer
View all (30 more)

4692
Fibroblast growth factor receptor 4
CD334, JTK2, TKF
Adenoid cystic carcinoma, Cholecystolithiasis, Focal segmental glomerulosclerosis, Liver cirrhosis, Prostatic neoplasms, Diabetes mellitus type 2

4693
Fibroblast growth factor receptor like 1
FGFR-5, FGFR5, FHFR
Atrial fibrillation, Bone fracture, Congenital diaphragmatic hernia, Gout, Obesity, Diabetes mellitus type 2, Wolf-hirschhorn syndrome

4694
Fibrinogen gamma chain
-
Blood coagulation disorder, Cardioembolic stroke, Thromboembolic pulmonary hypertension, Congenital afibrinogenemia, Congenital fibrinogen deficiency, Congenital hypofibrinogenemia, Cor pulmonale, Dysfibrinogenemia, Afibrinogenemia, Hypofibrinogenemia, Heart disease, Spastic paraplegia, Stomach neoplasms, Stroke, Thrombocytopenia
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4695
FGGY carbohydrate kinase domain containing
-
Astrocytoma, Bipolar disorder, Bronchopneumonia, Central nervous system cancer, Dementia, Glioma, Major depressive disorder, Obesity

4696
Fibrinogen like 1
HFREP1, HP-041, HPS, LFIRE-1, LFIRE1
Oligodendroglioma, Preeclampsia

4697
Fibrinogen like 2
T49, pT49
Allergic contact dermatitis, Liver cirrhosis

4698
FGR proto-oncogene, Src family tyrosine kinase
SRC2, c-fgr, c-src2, p55-Fgr, p55c-fgr, p58-Fgr, p58c-fgr
Liver cirrhosis, Psoriasis, Squamous cell carcinoma

4699
Fumarate hydratase
FMRD, HLRCC, HsFH, LRCC, MCL, MCUL1
Leiomyosarcoma, Major depressive disorder, Pheochromocytoma/paraganglioma syndrome

4700
Forkhead associated phosphopeptide binding domain 1
-
Color vision deficiency, Coronary aneurysm, Iga nephropathy, Pelvic organ prolapse