71
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|
|
RAB39A, member RAS oncogene family |
K28, RAB39 |
Curated: Uterine fibroid
Unreviewed: Cervical Cancer, Cervical Tumor, Cervix carcinoma, Malignant Neoplasm, Uterine neoplasm
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72
|
|
|
RAB39B, member RAS oncogene family |
BGMR, MRX72, WSMN, WSN, XLID72 |
Curated: Autism, Chromosome xq28 duplication syndrome, Craniofacial abnormalities, Developmental disability, Early-onset parkinsonism-intellectual disability syndrome, Epilepsy, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability, Parkinsonism with cognitive impairment, Waisman syndrome
Unreviewed: Aphasia, Attention Deficit Hyperactivity Disorder, Autism spectrum disorder, Cognition disorder, Development Disorder, Developmental Delay, DiGeorge Syndrome, Dolichocephaly, Dysarthria, Dyskinetic Syndrome, Facial paralysis, Frontal bossing, Hearing loss with stapes fixation, Impaired Cognition, Lewy Body Disease, Macrocephaly, Meckel Diverticulum, Mental retardation, Mental Retardation, X-Linked, Movement Disorders, Nephropathy with Pretibial Epidermolysis Bullosa and Deafness, Neurodegenerative disorder, Neurodegenerative Disorders, Neurofibromatosis, Neurosensory Hearing impairment, Non-Syndromic Intellectual Disability, X-Linked, Obesity, Pancreatic neoplasm, Parkinson disease, Parkinsonian disease, Secondary parkinson disease, Seizure, Speech Disorders, Stereotyped Behavior, Strabismus, Syndactyly Of The Toes
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73
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|
|
RAB3A, member RAS oncogene family |
- |
Curated: N/A
Unreviewed: Alzheimer disease, Anaplastic Ependymoma, Attention Deficit Hyperactivity Disorder, Autism, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Cone-rod dystrophy, Dementia, Diabetic Nephropathy, Endocrine system disease, Ependymoma, Glioblastoma, Glioma, Insulinoma, Leukemia, Liver carcinoma, Mental retardation, Myxopapillary Ependymoma, Neoplasms, Nervous System Neoplasms, Ovarian neoplasm, Pancreatic ductal carcinoma, Papillary Ependymoma, Pheochromocytoma, Senile Dementia, Senile Plaques
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74
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|
|
RAB3B, member RAS oncogene family |
- |
Curated: N/A
Unreviewed: Breast neoplasm, Diabetic neuropathy, Glioma, Hepatocellular carcinoma, Large cell carcinoma, Myeloid leukemia, Parkinson disease, Pheochromocytoma, Prostate cancer, Prostatic neoplasm, Small cell carcinoma, Squamous cell carcinoma
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75
|
|
|
RAB3C, member RAS oncogene family |
- |
Curated: Breast cancer, Major depressive disorder, Diabetes mellitus type 2
Unreviewed: Colorectal neoplasm, Congenital adrenal hyperplasia
|
76
|
|
|
RAB3D, member RAS oncogene family |
D2-2, GOV, RAB16, RAD3D |
Curated: Alzheimer disease
Unreviewed: B-Cell Lymphoma, Breast Cancer, Breast Carcinoma, Colorectal Cancer, Esophagus Neoplasm, Lung Cancer, Lung carcinoma, Lung neoplasms, Lupus Erythematosus, Malignant Neoplasm, Mammary Neoplasms, Melanoma, Mental Depression, Metabolic Syndrome, Neoplasms, Oligodendroglioma, Osteosarcoma, Pancreatic neoplasm, Sjogren syndrome, Triple negative breast cancer
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77
|
|
|
RAB3 GTPase activating protein catalytic subunit 1 |
MARTS2, P130, RAB3GAP, RAB3GAP130, WARBM1 |
Curated: Apert syndrome, Bilateral microphthalmos, Cataract-intellectual disability-hypogonadism syndrome, Congenital cataract, Congenital malformation syndromes predominantly affecting facial appearance, Congenital ptosis, Cryptophthalmos syndrome, Cryptorchidism, Cyclocephaly, Goldenhar syndrome, Hypertrichosis, Martsolf syndrome, Mobius syndrome, Movement disorder, Orofaciodigital syndrome, Intellectual disability, Uranostaphyloschisis, Warburg micro syndrome
Unreviewed: Abnormal dermatoglyphic pattern, Acquired Kyphoscoliosis, Agenesis Of Corpus Callosum, Alzheimer disease, Ataxia, Bone disease, Brachycephaly, Brain disease, Breast Carcinoma, Breast neoplasm, Carcinoma, Cardiomyopathy, Cataract, Central Visual Impairment, Cerebellar Hypoplasia, Cerebral Atrophy, Cerebral cortical atrophy, Colorectal Cancer, Colorectal neoplasm, Congenital Cataract, Congenital Hypoplasia Of Penis, Congenital kyphoscoliosis, Corneal disease, Deafness, Developmental Delay, Diabetes Mellitus, Dwarfism, Dysmorphic Features, Esophageal Carcinoma, Esophagus Neoplasm, Frontotemporal dementia, Fundus Coloboma, Gaucher disease, Glaucoma, Glioblastoma, Glycogen storage disease, High palate, Huntington disease, Hydronephrosis, Hypogonadism, Hypogonadotropic Hypogonadism, Hypoplasia Of Corpus Callosum, Intellectual developmental disorder, Keratoconus, Leukemia, Liver carcinoma, Lung adenocarcinoma, Lung carcinoma, Macrotia, Malignant Neoplasm, Martsolf Syndrome, Melanoma, Mental retardation, Micro Syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Mitral Valve Stenosis, Multiple Congenital Anomalies, Multiple Sclerosis, Neoplasms, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Optic Atrophy, Osteopenia, Osteoporosis, Ovarian cancer, Ovarian Carcinoma, Ovarian Epithelial carcinoma, Pachygyria, Papillary thyroid cancer, Parkinson disease, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Prostate cancer, Ptosis, Retinal coloboma, Retinoblastoma, Schizophrenia, Scoliosis, Senile Plaques, Skin abnormalities, Spastic diplegia, Warburg Micro Syndrome
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78
|
|
|
RAB3 GTPase activating non-catalytic protein subunit 2 |
MARTS1, RAB3-GAP150, RAB3GAP150, SPG69, WARBM2, p150 |
Curated: Apert syndrome, Attention deficit hyperactivity disorder, Spastic paraplegia, Cataract-intellectual disability-hypogonadism syndrome, Congenital cataract, Congenital malformation syndromes predominantly affecting facial appearance, Cryptophthalmos syndrome, Cyclocephaly, Goldenhar syndrome, Martsolf syndrome, Microphthalmos, Mobius syndrome, Orofaciodigital syndrome, Substance abuse, Warburg micro syndrome
Unreviewed: Abnormal dermatoglyphic pattern, Agenesis Of Corpus Callosum, Alzheimer disease, Amyotrophic Lateral Sclerosis, Ataxia, Blast phase chronic myelogenous leukemia, Brachycephaly, Brain disease, Cardiomyopathy, Cataract, Central Visual Impairment, Cerebral cortical atrophy, Cervix carcinoma, Congenital Cataract, Congenital Clubfoot, Congenital Epicanthus, Congenital Hypoplasia Of Penis, Congenital Pectus Carinatum, Congenital Pectus Excavatum, Congestive Heart Failure, Cryptorchidism, Developmental Delay, Drachtman Weinblatt Sitarz syndrome, Dwarfism, Frontotemporal dementia, Fundus Coloboma, Gaucher disease, Glaucoma, Glycogen storage disease, High palate, Huntington disease, Hydronephrosis, Hypogonadism, Hypogonadotropic Hypogonadism, Hypoplasia Of Corpus Callosum, Hypoplasia of the maxilla, Intellectual developmental disorder, Macrotia, Malignant Neoplasm, Martsolf Syndrome, Mental retardation, Micro Syndrome, Microcephaly, Microcornea, Micrognathism, Multiple Congenital Anomalies, Multiple Sclerosis, Neoplasms, Nervous System Diseases, Optic Atrophy, Ovarian cancer, Ovarian Carcinoma, Ovarian Epithelial carcinoma, Pachygyria, Parkinson Disease, Penis Agenesis, Polymicrogyria, Posteriorly Rotated Ear, Retinal coloboma, Scoliosis, Spastic diplegia, Spastic Paraplegia, Stomach Carcinoma, Stomach Neoplasms, Symmetrical Dyschromatosis Of Extremities, Tongue carcinoma, Tracheomalacia, Warburg Micro Syndrome
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79
|
|
|
RAB3A interacting protein like 1 |
GRAB |
Curated: Migraine, Schizophrenia
Unreviewed: Autism, Language development disorders
|
80
|
|
|
RAB3A interacting protein |
RABIN3, RABIN8 |
Curated: Atrial fibrillation, Color vision deficiency
Unreviewed: Colorectal neoplasm, Parkinson disease, Stomach Carcinoma, Stomach Neoplasms
|