Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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
6781 to 6790 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6781
Kinesin family member 3C
-
Amyotrophic lateral sclerosis, Atrial fibrillation, Motor neuron disease, Multiple myeloma, Diabetes mellitus type 2

6782
Kinesin family member 4A
KIF4, KIF4G1, MRX100, TMDI, XLID100
Hepatocellular carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Neurodevelopmental disorder, Hydrocephalus, Intellectual developmental disorder, x-linked, Obesity

6783
Kinesin family member 4B
-
Breast cancer, Coronary artery disease, Generalized anxiety disorder, Major depressive disorder, Scoliosis

6784
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, Hereditary motor and sensory neuropathies, Insomnia, Metabolic syndrome, Multiple sclerosis, Peripheral neuropathy, Schizophrenia, Hereditary spastic paraplegia
View all (1 more)

6785
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, Dilated cardiomyopathy, Contracture of multiple joints, Diabetes mellitus, Skeletal muscle disorder, Global developmental delay, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Osteoporosis-pseudoglioma syndrome, Schizophrenia

6786
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, Cortical dysplasia with other brain malformations, Developmental disability, Duane retraction syndrome, Major depressive disorder, Cortical development malformation, Microcephaly, Schizophrenia, Diabetes mellitus type 2

6787
Kinesin family member 6
C6orf102, dJ1043E3.1, dJ137F1.4, dJ188D3.1
Attention deficit hyperactivity disorder, Ischemic heart disease, Kidney disease, Color vision deficiency, Coronary artery disease, Diabetes mellitus type 2, Aortic dissection, Hypertension, Hypospadias, Kidney failure, Migraine, Myocardial infarction, Myocardial ischemia, Obesity, Orofacial cleft
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6788
Kinesin family member 7
ACLS, AGBK, HLS2, JBTS12, MMEDF, UNQ340
Acrocallosal syndrome, Bardet-biedl syndrome, Cerebellar ataxia, Cleft palate, Cleft lip, Color vision deficiency, Complete unilateral cleft lip, Desbuquois syndrome, Aplasia of the vermis, Hydrolethalus syndrome, Intellectual developmental disorder, Joubert syndrome, Male infertility testicular dysgenesis, Neurodevelopmental disorder, Nystagmus
View all (5 more)

6789
Kinesin family member 9
-
Breast cancer, Huntington disease, Scoliosis, Diabetes mellitus type 2

6790
Kinesin associated protein 3
FLA3, KAP-1, KAP-3, KAP3, SMAP, Smg-GDS, dJ190I16.1
Amyotrophic lateral sclerosis, Venous thromboembolism