1
|
|
|
Kalirin RhoGEF kinase |
ARHGEF24, CHD5, CHDS5, DUET, DUO, HAPIP, KALNC2, TRAD |
Alzheimer disease, Amyotrophic lateral sclerosis, Cerebral atherosclerosis, Ischemic stroke, Ischemic heart disease, Coronary artery disease, Diffuse large b-cell lymphoma, Generalized anxiety disorder, Glaucoma, Major depressive disorder, Myocardial infarction, Myocardial ischemia, Nephrotic syndrome, Neuroblastoma, Oligodendroglioma, Open angle glaucoma, Periodontal disease, Periodontitis, Rolandic epilepsy, Sarcoidosis, Schizophrenia, Stroke, Systemic lupus erythematosus, Depression, Venous thromboembolismView all (10 more) |
2
|
|
|
KN motif and ankyrin repeat domains 1 |
ANKRD15, CPSQ2, KANK |
Amyotrophic lateral sclerosis, Basal cell carcinoma, Cerebral palsy, Cholelithiasis, Keratinocyte carcinoma, Migraine, Multiple myeloma, Neurodevelopmental disorder, Obesity, Schizophrenia, Skin cancer, Skin neoplasms, Uterine fibroid |
3
|
|
|
KN motif and ankyrin repeat domains 2 |
ANKRD25, MXRA3, NPHS16, PPKWH, SIP |
Bronchial disease, Cardiovascular disease, Carpal tunnel syndrome, Coronary artery disease, Genetic steroid-resistant nephrotic syndrome, Heart failure, Hereditary steroid-resistant nephrotic syndrome, Metabolic syndrome, Nephrotic syndrome, Open angle glaucoma, Diabetes mellitus type 2, Woolly hair-palmoplantar keratoderma syndrome |
4
|
|
|
KN motif and ankyrin repeat domains 3 |
ANKRD47 |
|
5
|
|
|
KN motif and ankyrin repeat domains 4 |
ANKRD38, dJ1078M7.1 |
|
6
|
|
|
KAT8 regulatory NSL complex subunit 1 |
C17DELq21.31, CENP-36, DEL17Q21.31, KDVS, KIAA1267, MSL1v1, NSL1, hMSL1v1 |
17q21.31 microdeletion syndrome, Alzheimer disease, Androgenetic alopecia, Autism, Bladder calculus, Breast cancer, Cancer, Adenoid cystic carcinoma, Chromosome 17 deletion, Chromosome 17q21.31 deletion syndrome, Obstructive pulmonary disease, Colorectal cancer, Craniofacial abnormalities, Dysgenesis of corpus callosum, Estrogen-receptor negative breast cancer, Global developmental delay, Hypothyroidism, Idiopathic pulmonary fibrosis, Intellectual developmental disorder, Lewy body disease, Lung cancer, Major depressive disorder, Mood disorder, Nephrolithiasis, Neurotic disorder, Osteoarthritis, Ovarian cancer, Ovarian neoplasms, Ovarian serous carcinoma, Parkinson disease, Post-traumatic stress disorder, Prostate cancer, Pulmonary fibrosis, Schizophrenia, Squamous cell carcinoma, Diabetes mellitus type 2, Urolithiasis, koolen-de vries syndromeView all (23 more) |
7
|
|
|
KAT8 regulatory NSL complex subunit 1 like |
C2orf67, MSL1v2 |
|
8
|
|
|
KAT8 regulatory NSL complex subunit 3 |
KIAA1310, NSL3, Rcd1 |
|
9
|
|
|
Lysyl-tRNA synthetase 1 |
CMTRIB, DEAPLE, DFNB89, KARS, KARS2, KRS, LEPID |
Charcot-marie-tooth disease, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Congenital sensorineural hearing loss, Deafness, Deafness with congenital and adult-onset progressive leukodystrophy, Dejerine-sottas disease, Early onset progressive leukoencephalopathy-central nervous system calcification-hearing loss-visual impairment syndrome, Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome, Global developmental delay, Hearing loss, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Leukodystrophy, Nystagmus, Optic neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Nonsyndromic hearing loss, nonsyndromic genetic hearing lossView all (5 more) |
10
|
|
|
KASH domain containing 5 |
CCDC155, POF22, SPGF88 |
|