187831
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TBC1 domain family member 14 |
- |
Curated: Asthma
Unreviewed: N/A
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187832
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|
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TBC1 domain family member 15 |
RAB7-GAP |
Curated: Alzheimer disease, Schizophrenia
Unreviewed: Parkinson disease
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187833
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|
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TBC1 domain family member 16 |
- |
Curated: Color vision deficiency, Major depressive disorder, Migraine
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Epithelial ovarian carcinoma, Melanoma, Neoplasms, Ovarian cancer, Ovarian Epithelial carcinoma
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187834
|
|
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TBC1 domain family member 17 |
- |
Curated: N/A
Unreviewed: Vitiligo
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187835
|
|
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TBC1 domain family member 19 |
- |
Curated: Cardiovascular disease, Coronary artery disease, Heart failure, Hypertension, Myocardial infarction, Schizophrenia
Unreviewed: Cardiovascular Diseases
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187836
|
|
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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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187837
|
|
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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, Seizures, Developmental delay, Intellectual disability
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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187838
|
|
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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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187839
|
|
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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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187840
|
|
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TBC1D22A antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|