Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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

Showing genes starting with "F"

381 to 390 of 433 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
381	83656	FAM167A-AS1	FAM167A antisense RNA 1	C8orf12	Esophagus neoplasm, Lupus erythematosus
382	83706	FERMT3	FERM domain containing kindlin 3	KIND3, MIG-2, MIG2B, UNC112C, URP2, URP2SF	Anemia, Attention deficit hyperactivity disorder, Congenital osteopetrosis, Leukocyte adhesion deficiency, Osteopetrosis, Platelet-type bleeding disorder
383	83786	FRMD8	FERM domain containing 8	FKSG44, iTAP	Leukemia
384	83986	FAM234A	Family with sequence similarity 234 member A	C16orf9, ITFG3, gs19	Diabetes mellitus
385	84070	FAM186B	Family with sequence similarity 186 member B	C12orf25	Nephronophthisis
386	84075	FSCB	Fibrous sheath CABYR binding protein	C14orf155	Breast cancer
387	84085	FBXO30	F-box protein 30	Fbx30	Colorectal cancer
388	84140	FAM161A	FAM161 centrosomal protein A	RP28	Cataract, Cone-rod dystrophy, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy View all (3 more)
389	84188	FAR1	Fatty acyl-CoA reductase 1	CSPSD, MLSTD2, PFCRD, SDR10E1	Cataract, Developmental delay, Fatty acyl-coa reductase deficiency, Macrotia, Mental retardation, Microcephaly, Peroxisomal fatty acyl-coa reductase 1 disorder
390	8456	FOXN1	Forkhead box N1	FKHL20, RONU, TIDAND, TLIND, WHN	Alopecia, Autism, Aplasia of the thymus, Congenital alopecia totalis, Immunodeficiency, Immunologic deficiency syndromes, Macrocephaly, Nail dystrophy, Severe combined immunodeficiency disease, T-cell immunodeficiency, congenital alopecia and nail dystrophy

«««...37 383940 41...»»»