331
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Kinesin family member 19B, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
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332
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Kinesin family member 1A |
ATSV, C2orf20, HSN2C, MRD9, NESCAVS, SPG30, SPG30A, SPG30B, UNC104 |
Curated: 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 paraplegia, syndromic intellectual disability
Unreviewed: Acquired Porencephaly, Acrosteolysis, Amyloid angiopathy, Amyotrophic lateral sclerosis, Angina pectoris, Anhidrosis, Anodontia, Arthrogryposis multiplex congenita, Ataxia, Atrophy, Atrophy Of Corpus Callosum, Autism spectrum disorder, Benign Neoplasm, Brain disease, Brainstem Atrophy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma Of The Head And Neck, Cerebellar atrophy, Cerebellar diseases, Cerebellar hypoplasia, Cerebral Atrophy, Cerebral cortical atrophy, Colorectal neoplasm, Combined molybdoflavoprotein enzyme deficiency, Congenital Epicanthus, Corpus callosum agenesis, Cortical development malformation, Development Disorder, Developmental Delay, Diabetes, Diabetes Mellitus, Distal amyotrophy, Dysautonomia, Dystonia, Edema, Epilepsy, Gastroesophageal Reflux Disease, Glioma, Henoch-Schonlein Nephritis, Hydrocephalus, Hyperkinesia, Hypoparathyroidism, Hypoplasia Of Corpus Callosum, Impaired Cognition, Infantile Spasms, Language development disorders, Lymphedema, Microcephaly And Chorioretinopathy Syndrome, Macrotia, Malignant Neoplasm, Mental retardation, Microcephaly, Micropenis, Motor neuron atrophy, Movement Disorders, Multiple Congenital Anomalies, Nasopharyngeal Carcinoma, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy, Non-Syndromic Intellectual Disability, Optic Atrophy, Optic Neuropathy, Paraplegia, Paronychia Inflammation, PEHO Syndrome, Peripheral axonal neuropathy, Peripheral Neuropathy, Porencephalic cyst, Rett Syndrome, Scoliosis, Seizures, Sensorimotor neuropathy, Sensory Neuropathy, Hereditary, Spastic Paraplegia, Spinocerebellar Ataxia, Spondylometaphyseal dysplasia, Squamous cell carcinoma, Stroke, Thyroid cancer, Tooth abnormalities, Tuberous Sclerosis, Visual disorder, West Syndrome
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333
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|
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Kinesin family member 1B |
CMT2, CMT2A, CMT2A1, HMSNII, KLP, NBLST1 |
Curated: 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, Vitiligo, Charcot-Marie-Tooth disease type 2A1
Unreviewed: Adrenal Gland Pheochromocytoma, Agenesis Of Corpus Callosum, Amyloidosis, Amyotrophic Lateral Sclerosis, Anemia, Aniridia, Breast Cancer, Breast Carcinoma, Capillary Hemangioma Of Retina, Cataract, Cerebellar Diseases, Charcot-Marie-Tooth Disease, Complete Atrioventricular Block, Congenital glaucoma, Congenital Hypomyelinating Neuropathy, Congestive Heart Failure, Corneal dystrophy, Cranial nerve compression, Developmental Delay, Distal amyotrophy, Distal Spinal Muscular Atrophy, Dysautonomia, Episodic paroxysmal anxiety, Epithelial ovarian carcinoma, Extra-Adrenal Pheochromocytoma, Friedreich Ataxia, Ganglioneuroblastoma, Ganglioneuroma, Giant Axonal Neuropathy, Glioma, Glomerulonephritis, Glomerulosclerosis, Hearing Loss, Hemangioma, Henoch-Schonlein Nephritis, Hepatitis b, Hereditary Leber Optic Atrophy, Hereditary Liability To Pressure Palsies, Hereditary motor and sensory neuropathy, Hereditary Motor And Sensory Neuropathy With Optic Atrophy, Hereditary Paraganglioma-Pheochromocytoma Syndromes, Hereditary Pheochromocytoma-Paraganglioma, Hereditary sensory and autonomic neuropathy, Horner Syndrome, Hypercalcemia, Hypertension, Hypertensive Retinopathy, Inherited Peripheral Neuropathy, Liver carcinoma, Liver Cirrhosis, Malignant Neoplasm, Medulloblastoma, Mental retardation, Microcephaly, Motor nerve neuritis, Motor Neuron Disease, Multiple Sclerosis, Myopathy, Neoplasms, Nervous System Diseases, Nervous System Disorder, Neural Crest Tumor, Neurodegenerative Disorders, Neuromuscular Diseases, Neuronopathy, Neuropathy, Neuropathy Ataxia And Retinis Pigmentosa, Oligodendroglioma, Opsoclonus, Optic Atrophy, Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy, Optic Neuropathy, Ovarian cancer, Ovarian Epithelial carcinoma, Panic Disorder, Paraganglioma, Paraganglioma of head and neck, Paroxysmal Hypertension, Partial Paralysis Vocal Cords, Peripheral axonal atrophy, Peripheral axonal neuropathy, Peripheral Neuropathy, Polyneuropathy, Pulsatile Tinnitus, Renal Artery Stenosis, Renal Carcinoma, Renal cell carcinoma, Russell-Silver Syndrome, Sensory neuropathy, Sinus Tachycardia, Spastic Paraplegia, Spinal cord compression, Spinal Muscular Atrophy, Spondylometaphyseal dysplasia, Stomach Carcinoma, Stomach Neoplasms, Stroke, Syndactyly, Vocal Cord Paralysis
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334
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|
|
Kinesin family member 1C |
LTXS1, SATX2, SAX2, SPAX2, SPG58 |
Curated: Ataxia, spastic, autosomal recessive, Spastic paraplegia, Cerebellar ataxia, Intellectual developmental disorder, Keratoconus, Obesity, Scoliosis, Spastic ataxia, Hereditary spastic paraplegia
Unreviewed: Ataxia, Ataxia, spastic with optic atrophy and mental retardation, Atrial myxoma, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar Diseases, Cerebral Atrophy, Demyelinating diseases, Developmental Delay, Distal amyotrophy, Dwarfism, Dysarthria, Dystonia, Henoch-Schonlein Nephritis, Horizontal nystagmus, Hypodontia, Mental retardation, Microcephaly, Motor neuron disease, Movement disorder, Nervous System Diseases, Neurodegenerative disorder, Spastic Ataxia, Spastic Paraplegia, Tremor
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335
|
|
|
KIF1C antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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336
|
|
|
Kinesin family member 20A |
MKLP2, RAB6KIFL, RCM6 |
Curated: Hepatocellular carcinoma, Cardiomyopathy, Congenital heart disease, Restrictive cardiomyopathy
Unreviewed: Adenocarcinoma, Aortic dissection, Arthritis, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Charcot-Marie-Tooth Disease, Colorectal Cancer, Colorectal neoplasm, Endometriosis, Epithelial ovarian carcinoma, Glioblastoma, Glioma, Hematologic Neoplasms, Hepatitis b, Histiocytoid Cardiomyopathy, Intervertebral disc disease, Kidney neoplasm, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lymphatic metastasis, Malignant Neoplasm, Melanocytic nevus, Melanoma, Meningioma, Mesothelioma, Myeloid Leukemia, Nasopharyngeal Cancer, Nasopharyngeal carcinoma, Neoplasms, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Prostate cancer, Prostatic neoplasm, Renal Carcinoma, Renal cell carcinoma, Retinoblastoma, Squamous cell carcinoma, Stomach Carcinoma, Stomach Neoplasms, Syndromic microphthalmia, Urinary bladder cancer, Urinary bladder neoplasms, Uterine neoplasm
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337
|
|
|
Kinesin family member 20B |
CT90, KRMP1, MPHOSPH1, MPP-1, MPP1 |
Curated: 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 2
Unreviewed: Adenocarcinoma, Ankylosing Spondylitis, Arthritis, beta Thalassemia, Bladder carcinoma, Bladder Neoplasm, Blast phase chronic myelogenous leukemia, Breast Cancer, Breast Carcinoma, Carcinoma, Colorectal Cancer, Colorectal neoplasm, Diabetes Mellitus, Esophageal neoplasm, Fatty Liver, Glioblastoma, Hereditary Spherocytosis, Hodgkin Disease, Leukemia, Liver Cancer, Liver carcinoma, Lung Cancer, Lung Neoplasms, Lupus Erythematosus, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Malignant Neoplasm, Malignant Neoplasm Of Tongue, Microcephaly, Multiple Sclerosis, Myeloid Leukemia, Neoplasms, Neurodegenerative Disorders, Osteosarcoma, Pulmonary Emphysema, Renal Carcinoma, Respiratory Distress Syndrome, Rheumatoid arthritis, Sarcoidosis, Sickle cell anemia, T-cell leukemia, Testicular Germ Cell Tumor, Testicular neoplasm, Urinary bladder cancer, Urothelial Carcinoma
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338
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|
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Kinesin family member 21A |
CFEOM1, FEOM1, FEOM3A |
Curated: Arthrogryposis multiplex congenita, Congenital fibrosis of extraocular muscles, Fetal akinesia deformation sequence, Pena-shokeir syndrome , Small cell lung carcinoma
Unreviewed: Aniridia, Brain disease, Congenital bilateral ptosis, Congenital ocular coloboma, Corneal ulcer, Corpus callosum agenesis, Developmental disability, Down Syndrome, Duane Retraction Syndrome, Esotropia, Exotropia, Fibrosis Of Extraocular Muscles, Lung carcinoma, Malignant Neoplasm, Mobius Syndrome, Myopathy, Neoplasms, Neurodevelopmental Disorders, Oculomotor nerve palsy, Ophthalmoplegia, Pancreatic ductal carcinoma, Peripheral nervous system disease, Ptosis, Schizophrenia, Sensory exotropia, Strabismus, Syndromic microphthalmia, Uranostaphyloschisis
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339
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|
|
Kinesin family member 21B |
- |
Curated: 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
Unreviewed: Alzheimer disease, Ankylosing Spondylitis, Anterior uveitis, Autism Spectrum Disorder, Autoimmune disease, Autoimmune Diseases, Celiac disease, Crohn Disease, Demyelinating diseases, Hepatocellular carcinoma, Inflammatory Bowel Disease, Medulloblastoma, Multiple Sclerosis, Neurodegenerative disorder, Neurodegenerative Disorders, Parkinson disease, Prostatic neoplasm, Stomach neoplasms
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340
|
|
|
Kinesin family member 22 |
A-328A3.2, KID, KNSL4, OBP, OBP-1, OBP-2, SEMDJL2 |
Curated: Alzheimer disease, Desbuquois syndrome, Larsen syndrome, Spondyloepimetaphyseal dysplasia
Unreviewed: Adenocarcinoma, Agenesis Of Corpus Callosum, Anxiety Disorder, Aplasia Cutis Congenita, Arthritis, Bipolar Disorder, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Congenital diaphragmatic hernia, Congenital Ichthyosis, Coronary Heart Disease, Developmental Delay, Developmental dysplasia of the hip, Dislocated radial head, Dwarfism, Epilepsy, FG Syndrome, Frontal bossing, Head and neck cancer, Head And Neck Carcinoma, Ichthyosis, Immunologic Deficiency Syndromes, Inflammatory Bowel Disease, Irritable Bowel Syndrome, Keratitis, Keratitis ichthyosis and deafness syndrome, Laryngostenosis, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung Neoplasms, Lymphatic metastasis, Macrocephaly, Malignant Neoplasm, Medulloblastoma, Melanoma, Mesothelioma, Micromelia, Nail Diseases, Nail dysplasia, Neoplasms, Obsessive-Compulsive Disorder, Osteochondrodysplasia, Osteosarcoma, Pancreatic neoplasm, Phyllodes Tumor, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Renal Carcinoma, Rhabdomyosarcoma, Sarcoma, Scoliosis, Senter Syndrome, Skeletal Dysplasia, Spina Bifida, Spondyloepimetaphyseal Dysplasia With Joint Laxity, Spondyloepimetaphyseal Dysplasia With Multiple Dislocations, Stomach neoplasms, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Triple Negative Breast Neoplasms, Urinary bladder cancer
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