361
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|
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Kinesin family member 4A |
KIF4, KIF4G1, MRX100, TMDI, XLID100 |
Curated: Hepatocellular carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Neurodevelopmental disorder, Hydrocephalus, Intellectual developmental disorder, x-linked, Obesity, complex neurodevelopmental disorder with or without congenital anomalies
Unreviewed: Agenesis Of Corpus Callosum, Aneuploidy, Brain disease, Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Cholangiocarcinoma, Colorectal Cancer, Colorectal neoplasm, Congenital abnormalities, Congenital anomalies of the kidney and urinary tract, Congenital heart defect, Developmental disability, Endometrial neoplasm, Ependymoma, Epilepsy, Epithelial ovarian carcinoma, Esophageal squamous cell carcinoma, Eye abnormalities, Glioblastoma, Glioma, Intellectual developmental disorder, Language development disorders, Lip and Oral Cavity Carcinoma, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Lymphatic metastasis, Lymphedema, Malignant Neoplasm, Malignant neoplasm of mouth, Meningioma, Mental retardation, Mental Retardation, X-Linked, Mouth neoplasm, Multicystic renal dysplasia, Neoplasms, Osteosarcoma, Ovarian neoplasm, Prostate cancer, Renal cell carcinoma, Retinoblastoma, Sarcoma, Squamous cell carcinoma, Triple Negative Breast Neoplasms, Urinary bladder neoplasms, Urogenital abnormalities
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362
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|
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Kinesin family member 4B |
- |
Curated: Breast cancer, Coronary artery disease, Generalized anxiety disorder, Major depressive disorder, Scoliosis
Unreviewed: Hepatocellular carcinoma, Liver carcinoma
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363
|
|
|
Kinesin family member 4C, pseudogene |
KIF4P1 |
Curated: N/A
Unreviewed: N/A
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364
|
|
|
Kinesin family member 5A |
ALS25, D12S1889, MY050, NEIMY, NKHC, SPG10 |
Curated: 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, Diabetes mellitus type 2, amyotrophic lateral sclerosis, susceptibility to, 25, inherited neurodegenerative disorder
Unreviewed: Alzheimer disease, Amyotrophic Lateral Sclerosis, Apnea, Arthritis, Autoimmune Diseases, Basal ganglia disease, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Central Visual Impairment, Charcot-Marie-Tooth Disease, Critical illness, Deglutition disorder, Developmental disability, Diabetes Mellitus, Diabetes mellitus, type 1, Distal lower limb amyotrophy, Dupuytren Contracture, Dysautonomia, Dysphagia, Epilepsy, Essential tremor, Frontotemporal dementia, Henoch-Schonlein Nephritis, Hereditary sensory and motor neuropathy, Immune System Diseases, Impaired Cognition, Infantile spasms, Intellectual developmental disorder, Juvenile arthritis, Lateral Sclerosis, Leukodystrophy, Leukoencephalopathy, Limb amyotrophy, Lissencephaly, Liver neoplasm, Lupus Erythematosus, Lupus Vulgaris, Mental retardation, Microcephaly, Mitochondrial disease, Multiple Sclerosis, Myoclonic Epilepsy, Myoclonus, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neuropathy, Nystagmus, Paraplegia, Parkinson Disease, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Pica, Psoriatic Arthritis, Ptosis, Rod-cone dystrophy, Scoliosis, Secondary parkinson disease, Sensorimotor neuropathy, Spastic Paraplegia, Spinal muscular atrophy, Spinocerebellar ataxia, Spondylometaphyseal dysplasia, Urinary bladder cancer, Vulval varices
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365
|
|
|
Kinesin family member 5B |
HEL-S-61, KINH, KNS, KNS1, UKHC |
Curated: 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
Unreviewed: Adenocarcinoma, Amyotrophic Lateral Sclerosis, Attention Deficit Hyperactivity Disorder, Brain injuries, Breast Cancer, Breast Carcinoma, Carcinoma, Developmental Delay, Diabetes Mellitus, Endometrial Cancer, Endometrial carcinoma, Fibrosarcoma, Glioblastoma, Glioma, Henoch-Schonlein Nephritis, Hirschsprung disease, Histiocytosis, Hypoplasia Of Corpus Callosum, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung Neoplasms, Malignant Neoplasm, Medullary thyroid cancer, Megalencephaly, Polymicrogyria, Polydactyly, Hydrocephalus Syndrome, Melanoma, Multiple myeloma, Myeloproliferative disorder, Neoplasms, Neuroblastoma, Neurodegenerative disorder, Osteosarcoma, Pancreatic neoplasm, Papillary thyroid carcinoma, Renal cell carcinoma, Sarcoma, Sleep deprivation, Spastic paraplegia, Spondylometaphyseal dysplasia, Squamous cell carcinoma, Uterine neoplasm, Varicocele
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366
|
|
|
Kinesin family member 5C |
CDCBM2, KINN, NKHC, NKHC-2, NKHC2 |
Curated: 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
Unreviewed: Arthrogryposis multiplex congenita, Benign neonatal epilepsy, Brain malformation, Congenital Microcephaly, Cortical Dysplasia, Cortical Dysplasia With Other Brain Malformations, Developmental Delay, Epilepsy, Glioblastoma, Henoch-Schonlein Nephritis, Hypoplasia Of Corpus Callosum, Language development disorders, Lissencephaly, Macular corneal dystrophy, Macular dystrophy, Malformation of cortical development, Medullary thyroid cancer, Mental retardation, Microlissencephaly, Neoplasms, Neurodevelopmental Disorders, Pachygyria, Pena Shokeir syndrome, Polymicrogyria, Spastic paraplegia, Spastic Quadriplegia, Spondylometaphyseal dysplasia
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367
|
|
|
KIF5C antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
368
|
|
|
Kinesin family member 6 |
C6orf102, dJ1043E3.1, dJ137F1.4, dJ188D3.1 |
Curated: 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, Scoliosis, Smooth surface dental caries
Unreviewed: Alzheimer disease, Arteriosclerosis, Atherosclerosis, Azoospermia, Breast Cancer, Cardiovascular disease, Cardiovascular Diseases, Cognition disorder, Cognitive disorder, Coronary Arteriosclerosis, Coronary Heart Disease, Coronary Syndrome, Dental caries, Diabetes Mellitus, Diabetes mellitus, type 2, Dyslipidemias, Extravasation of diagnostic and therapeutic materials, Hypercholesterolemia, Hyperlipoproteinemia, Male infertility, Mental retardation, Myocardial Infarction, Stroke, Thoracic aortic aneurysm
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369
|
|
|
Kinesin family member 7 |
ACLS, AGBK, HLS2, JBTS12, MMEDF, UNQ340 |
Curated: 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, Obesity, Orofaciodigital syndrome, Polydactyly, Strabismus, Postaxial polydactyly
Unreviewed: Absence Of Septum Pellucidum, Acrocallosal Syndrome, Agenesis Of Corpus Callosum, Anencephaly, Arachnoid cyst, Arrhinencephaly, Arthritis, Attention Deficit Hyperactivity Disorder, Bardet-Biedl Syndrome, Bone disease, Brachydactyly, Brain atrophy, Brain disease, Camptodactyly of fingers, Cerebellar vermis agenesis, Cerebral Atrophy, Choriocarcinoma, Ciliopathies, Ciliopathy, Clinodactyly, Colpocephaly, Congenital Atresia Of Trachea, Congenital diaphragmatic hernia, Congenital Epicanthus, Congenital Exomphalos, Congenital heart defects, Congenital malrotation of intestine, Congenital Pectus Carinatum, Congenital Pectus Excavatum, Cryptorchidism, Dandy-Walker Syndrome, Developmental Delay, Disorder Of Eye, Dwarfism, Dysmorphic Features, Epithelial ovarian carcinoma, Esotropia, Facial dysmorphism, Foot Polydactyly, Frontal bossing, Gestational trophoblastic disease, Gestational Trophoblastic Neoplasms, Hearing Loss, Heart Septal Defects, Hereditary Hemochromatosis, High palate, Hydatidiform mole, Hydrocephalus, Hydrolethalus Syndrome, Hypertension, Hypoplasia Of The Optic Nerve, Hypospadias, Hypothalamic Hamartomas, Hypotonia, Imperforate anus, Joubert syndrome, Digenic, Laryngomalacia, Lung neoplasms, Macrocephaly, Macrocephaly With Multiple Epiphyseal Dysplasia And Distinctive Facies, Malformation of cortical development, Melanoma, Mental Disorders, Mental retardation, Micrognathism, Micromelia, Microphthalmos, Motor delay, Multiple Congenital Anomalies, Multiple Epiphyseal Dysplasia, Muscular dystrophy, Neoplasms, Osteochondrodysplasias, Ovarian cancer, Ovarian Epithelial carcinoma, Polycystic Ovary Syndrome, Polydactyly Of Toes, Postaxial hand polydactyly, Prostate cancer, Prostatic Neoplasms, Ptosis, Radial Polydactyly, Renal agenesis, Retinitis Pigmentosa, Submucosal cleft palate, Syndactyly, Syndactyly of fingers, Syndactyly Of The Toes, Syndromic microphthalmia, Tumor, Uranostaphyloschisis, Uterine Anomalies, Ventricular tachycardia
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370
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Kinesin family member 9 |
- |
Curated: Breast cancer, Huntington disease, Scoliosis, Diabetes mellitus type 2
Unreviewed: Coronary Heart Disease, Diabetes Mellitus, Diabetes mellitus, type 2, Glioblastoma, Hepatocellular carcinoma, Inflammatory bowel disease
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