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

6761 to 6770 of 15380 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
6761	146909	KIF18B	Kinesin family member 18B	-	Hepatocellular carcinoma, Endometriosis, Melanoma, Migraine, Prostate cancer
6762	124602	KIF19	Kinesin family member 19	KIF19A	Non-immune hydrops fetalis, Major depressive disorder
6763	547	KIF1A	Kinesin family member 1A	ATSV, C2orf20, HSN2C, MRD9, NESCAVS, SPG30, SPG30A, SPG30B, UNC104	Autism, Nonsyndromic intellectual disability, Spastic paraplegia, Coronary artery disease, Developmental disability, Diabetes mellitus, Hereditary motor and sensory neuropathies, Hereditary sensory and autonomic neuropathy, Insomnia, Intellectual developmental disorder, Major depressive disorder, Peho syndrome, Psoriasis, Sensory neuropathy, Spastic ataxia, Hereditary spastic paraplegia View all (1 more)
6764	23095	KIF1B	Kinesin family member 1B	CMT2, CMT2A, CMT2A1, HMSNII, KLP, NBLST1	Alzheimer disease, Arthrogryposis multiplex congenita, Atrial fibrillation, Charcot-marie-tooth disease, Breast cancer, Obstructive pulmonary disease, Congenital hemihypertrophy, Congenital joint contractures, Dejerine-sottas disease, Global developmental delay, Hepatocellular carcinoma, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Intellectual developmental disorder, Meniere disease View all (8 more)
6765	10749	KIF1C	Kinesin family member 1C	LTXS1, SATX2, SAX2, SPAX2, SPG58	Ataxia, spastic, autosomal recessive, Spastic paraplegia, Cerebellar ataxia, Intellectual developmental disorder, Keratoconus, Obesity, Scoliosis, Spastic ataxia, Hereditary spastic paraplegia
6766	10112	KIF20A	Kinesin family member 20A	MKLP2, RAB6KIFL, RCM6	Hepatocellular carcinoma, Cardiomyopathy, Congenital heart disease, Restrictive cardiomyopathy
6767	9585	KIF20B	Kinesin family member 20B	CT90, KRMP1, MPHOSPH1, MPP-1, MPP1	Androgenetic alopecia, Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma, Ocular hypertension, Ovarian cancer View all (5 more)
6768	55605	KIF21A	Kinesin family member 21A	CFEOM1, FEOM1, FEOM3A	Arthrogryposis multiplex congenita, Congenital fibrosis of extraocular muscles, Fetal akinesia deformation sequence, Pena-shokeir syndrome , Small cell lung carcinoma
6769	23046	KIF21B	Kinesin family member 21B	-	Ankylosing spondylitis, Attention deficit hyperactivity disorder, Autism, Biliary cirrhosis, Bipolar disorder, Ulcerative colitis, Crohn disease, Inflammatory bowel disease, Long qt syndrome, Macrogyria, Major depressive disorder, Neurodevelopmental disorder, Biliary cholangitis, Schizophrenia
6770	3835	KIF22	Kinesin family member 22	A-328A3.2, KID, KNSL4, OBP, OBP-1, OBP-2, SEMDJL2	Alzheimer disease, Desbuquois syndrome, Larsen syndrome, Spondyloepimetaphyseal dysplasia

«««...675 676677678 679...»»»