211
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|
|
TBC1 domain family member 2 |
PARIS-1, PARIS1, TBC1D2A |
Curated: Duodenitis, Hypertrophic cardiomyopathy, Post-traumatic stress disorder, Prostatic neoplasms
Unreviewed: Hereditary hyperferritinemia with congenital cataracts, Intracranial aneurysm, Melanoma, Multiple Sclerosis, Prostate cancer, Prostatic Neoplasms, Stress Disorder
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212
|
|
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TBC1 domain family member 20 |
C20orf140, WARBM4 |
Curated: Apert syndrome, Congenital malformation syndromes predominantly affecting facial appearance, Cryptophthalmos syndrome, Cyclocephaly, Goldenhar syndrome, Mobius syndrome, Orofaciodigital syndrome, Warburg micro syndrome
Unreviewed: Ataxia, Brain disease, Cataract, Central Visual Impairment, Cerebellar atrophy, Cerebral cortical atrophy, Congenital Hypoplasia Of Penis, Cryptorchidism, Developmental Delay, Dwarfism, Frontotemporal dementia, Fundus Coloboma, Gaucher disease, Glaucoma, Glycogen storage disease, High palate, Huntington disease, Hydronephrosis, Hypoplasia Of Corpus Callosum, Intellectual developmental disorder, Macrotia, Mental retardation, Micro Syndrome, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Microstomia, Nervous System Diseases, Optic Atrophy, Pachygyria, Parkinson disease, Penis Agenesis, Ptosis, Retinal coloboma, Scoliosis, Spastic Quadriplegia, Warburg Micro Syndrome
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213
|
|
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TBC1 domain family member 21 |
MgcRabGAP |
Curated: Bipolar disorder, Kidney disease, Color vision deficiency, Conotruncal cardiac defect, Diabetic neuropathy, Insomnia, Irritable bowel syndrome, Major depressive disorder, Metabolic syndrome, Myopathy, Neurotic disorder, Oligodendroglioma, Scoliosis, Diabetes mellitus type 2
Unreviewed: Exfoliation Syndrome
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214
|
|
|
TBC1 domain family member 22A |
C22orf4, HSC79E021 |
Curated: Colorectal cancer, Ovarian cancer
Unreviewed: Bipolar Disorder, Cardiovascular disease, Generalized epilepsy with febrile seizures plus, Hepatocellular carcinoma, Hypertension, Metabolic syndrome, Obesity, Pulmonary arterial hypertension, Schizophrenia
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215
|
|
|
TBC1D22A antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
216
|
|
|
TBC1D22A divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
217
|
|
|
TBC1 domain family member 22B |
C6orf197 |
Curated: Central nervous system cancer, Glioblastoma, Glioma
Unreviewed: Triple negative breast cancer, Venous thromboembolism
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218
|
|
|
TBC1 domain family member 23 |
NS4ATP1, PCH11 |
Curated: Central nervous system cancer, Glioma, Pontocerebellar hypoplasia
Unreviewed: Congenital Clubfoot, Congenital ocular coloboma, Developmental Delay, Dwarfism, Dysarthria, Dysphagia, Esotropia, Hyperopia, Hypoplasia Of Corpus Callosum, Macrotia, Mental retardation, Microcephaly, Pontoneocerebellar hypoplasia, Stereotyped Behavior
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219
|
|
|
TBC1 domain family member 24 |
DEE16, DFNA65, DFNB86, DOORS, EIEE16, EIM, EPRPDC, FIME, TLDC6 |
Curated: Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic hearing loss, Nonsyndromic intellectual disability, Cerebellar atrophy, Congenital neurologic anomalies, Deafness, Deafness with congenital onychodystrophy, Deafness, onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome, Developmental and epileptic encephalopathy, Digitrenocerebral syndrome, Doors syndrome, Dysarthria, Epilepsy of infancy with migrating focal seizures, Infantile myoclonic epilepsy, Rolandic epilepsy, Focal epilepsy-intellectual disability-cerebro-cerebellar malformation, Global developmental delay, Hearing loss, Intellectual developmental disorder, Malignant migrating partial seizures of infancy, Movement disorder, Nystagmus, Parkinson disease, Periodic paralysis, Progressive myoclonic epilepsy, Specific learning disability, nonsyndromic genetic hearing loss
Unreviewed: Action Myoclonus-Renal Failure Syndrome, Adrenal hyperplasia, Alternating Hemiplegia, Alternating hemiplegia of childhood, Ambiguous Genitalia, Anonychia, Arrhinencephaly, Attention Deficit Hyperactivity Disorder, Autism, Brachycephaly, Brachydactyly, Brain disease, Breast Cancer, Breast Carcinoma, Camptodactyly of fingers, Cataract, Cerebral Atrophy, Cerebral palsy, Classical Hodgkin lymphoma, Colitis, Congenital adrenal hyperplasia, Congenital Clubfoot, Congenital Epicanthus, Congenital Hypothyroidism, Congenital nystagmus, Dandy-Walker Syndrome, Dentatorubral Pallidoluysian Atrophy, Developmental Delay, Developmental disability, Developmental regression, Digitorenocerebral Syndrome, DOORS Syndrome, Double Outlet Right Ventricle, Dyscognitive seizures, Dystonia, Epilepsia Partialis Continua, Epilepsy, Epilepsy, Rolandic With Paroxysmal Exercise-Induced Dystonia And Writer`S Cramp, Epileptic encephalopathy, Erythema nodosum, Febrile seizures, Focal Epilepsy-Intellectual Disability-Cerebro-Cerebellar Malformation, Frontal bossing, Gastroesophageal Reflux Disease, Gonadal Dysgenesis, Headache, Hearing Loss, Hemifacial seizures, Hemiplegia, Hereditary Leber Optic Atrophy, High palate, Horizontal nystagmus, Hydronephrosis, Inborn Errors Of Metabolism, Inclusion-Body Disease, Infantile Spasms, Inflammatory Bowel Disease, Language Disorders, Lumbar scoliosis, Malignant Neoplasm, May-White Syndrome, Mental retardation, Microcephaly, Movement Disorders, Myoclonic Epilepsy, Myoclonic Seizures, Myopia, Nail Diseases, Nail dysplasia, Nail dystrophy, Neoplasms, Nephrocalcinosis, Nervous System Diseases, Nervous System Disorder, Neurodevelopmental Disorders, Nicolaides Baraitser Syndrome, Non-Syndromic Sensorineural Deafness, Nonconvulsive status epilepticus, Nonsyndromic Deafness, Optic Atrophy, Parkinson Disease, Periodic Paralysis, Photosensitive tonic-clonic seizures, Polymicrogyria, Polyneuropathy, Progressive Myoclonic Epilepsy With Dystonia, Proteasome-associated autoinflammatory syndrome, Psychiatric disorders, Rolandic Epilepsy-Paroxysmal Exercise-Induced Dystonia-Writer`s Cramp Syndrome, Sagittal craniosynostosis, Seizure, Seizures, Sensorineural hearing loss, Sirenomelia, Spasms X-Linked, Spina bifida occulta, Status Epilepticus, Strabismus, Strawberry Nevus Of Skin, Thrombocytosis, Ulcerative colitis, Usher syndrome, Uveitis, West Syndrome, Writer`s Cramp
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220
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|
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TBC1 domain family member 25 |
MG81, OATL1 |
Curated: Mood disorder
Unreviewed: Alveolar Sarcoma, Anxiety Disorder, Mental retardation, Mood Disorder, Neoplasms, Papillary Renal Carcinoma, Synovial sarcoma, Wiskott-Aldrich Syndrome
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