Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "K"
151 to 160 of 320 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
Ketohexokinase
FRUCTU
Fructokinase deficiency, Fructosuria

152
Kinesin family member 2A
CDCBM3, HK2, KIF2
Complex cortical dysplasia with other brain malformations, Cortical dysplasia with other brain malformations, Hypertension, Insomnia, Major depressive disorder, Cortical development malformation, Microcephaly, Post-traumatic stress disorder, Schizophrenia

153
Kinesin family member 3C
-
Amyotrophic lateral sclerosis, Atrial fibrillation, Motor neuron disease, Multiple myeloma, Diabetes mellitus, type 2

154
Kinesin family member 5A
ALS25, D12S1889, MY050, NEIMY, NKHC, SPG10
Amyotrophic lateral sclerosis, Rheumatoid arthritis, Auditory neuropathy, Charcot-marie-tooth disease, Spastic paraplegia, Dyskinesia, Frontotemporal dementia with or without amyotrophic lateral sclerosis, Genetic neurodegenerative disease, Insomnia, Metabolic syndrome, Multiple sclerosis, Peripheral neuropathy, Schizophrenia, Hereditary spastic paraplegia, Diabetes mellitus, type 2

155
Kinesin family member 5B
HEL-S-61, KINH, KNS, KNS1, UKHC
Attention deficit hyperactivity disorder, Bipolar disorder, Bone fragility with contractures, arterial rupture, and deafness, Brain atrophy, Non-small-cell lung carcinoma, Cardiomyopathy, Diabetes mellitus, Global developmental delay, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Osteoporosis-pseudoglioma syndrome, Schizophrenia

156
Kinesin family member 5C
CDCBM2, KINN, NKHC, NKHC-2, NKHC2
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Breast cancer, Complex cortical dysplasia with other brain malformations, Cortical dysplasia with other brain malformations, Developmental disability, Duane retraction syndrome, Major depressive disorder, Cortical development malformation, Microcephaly, Schizophrenia, Diabetes mellitus, type 2

157
Killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1
CD158A, KIR-K64, KIR221, KIR2DL3, NKAT, NKAT-1, NKAT1, p58.1
Keratoconus

158
Killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 1
CD158H, CD158a, p50.1

159
Killer cell immunoglobulin like receptor, two Ig domains and short cytoplasmic tail 4 (gene/pseudogene)
CD158I, KIR-2DS4, KIR1D, KIR412, KKA3, NKAT-8, NKAT8
Severe acute respiratory syndrome

160
Killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1
CD158E1, KIR, KIR2DL5B, KIR3DL1/S1, NKAT-3, NKAT3, NKB1, NKB1B
Hepatitis c, Human immunodeficiency virus infection, Hydatidiform mole, Keratoconus, Tuberculoma