201
|
|
|
Kinesin family member 18B |
- |
|
202
|
|
|
Kinesin family member 19 |
KIF19A |
|
203
|
|
|
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 paraplegiaView all (1 more) |
204
|
|
|
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, Multiple sclerosis, Neuroblastoma, Peroneal muscle atrophy, Pheochromocytoma, Roussy-levy syndrome, Scoliosis, Spinal muscular atrophy, VitiligoView all (8 more) |
205
|
|
|
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 |
206
|
|
|
Kinesin family member 20A |
MKLP2, RAB6KIFL, RCM6 |
|
207
|
|
|
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, Ovarian serous carcinoma, Pancreatic cancer, Prostate cancer, Squamous cell carcinoma, Diabetes mellitus type 2View all (5 more) |
208
|
|
|
Kinesin family member 21A |
CFEOM1, FEOM1, FEOM3A |
|
209
|
|
|
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 |
210
|
|
|
Kinesin family member 22 |
A-328A3.2, KID, KNSL4, OBP, OBP-1, OBP-2, SEMDJL2 |
|