187451
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SPT5 homolog, DSIF elongation factor subunit |
SPT5, SPT5H, Tat-CT1 |
Curated: N/A
Unreviewed: Beta thalassemia, Breast neoplasm, Colorectal neoplasm, Malignant Neoplasm, Neoplasms, Neurodegenerative disorder, Neurodegenerative Disorders
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187452
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SPT6 homolog, histone chaperone and transcription elongation factor |
SPT6, SPT6H, emb-5 |
Curated: Gout
Unreviewed: Breast neoplasm, Squamous cell carcinoma, Testicular germ cell tumor
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187453
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SPT7 like, STAGA complex subunit gamma |
FZPS, SPT7L, STAF65, STAF65(gamma), STAF65G, SUPT7H |
Curated: Lipodystrophy
Unreviewed: Cutis laxa, Developmental disability, Esophageal squamous cell carcinoma, Lung adenocarcinoma, Lymphoma, Mycosis fungoides, T-Cell Lymphoma/Leukemia
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187454
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Suv3 like RNA helicase |
SUV3 |
Curated: Congenital skin anomaly, Ichthyosis, Sarcopenia, Skin abnormalities, Xeroderma
Unreviewed: Alopecia, Alopecia, Male Pattern, Androgenetic Alopecia, Ataxia, Autoimmune disease, Calcinosis, Chronic obstructive pulmonary disease, Cognition disorder, Congenital abnormalities, Intervertebral disc displacement, Mammary Neoplasms, Mitochondrial disease, Mitochondrial Diseases, Neoplasms, Neurodegenerative disorder, Nystagmus, Optic atrophy, Paraparesis, Pseudopelade, Retinitis pigmentosa, Skin disease, Spinocerebellar ataxia, Stomach neoplasms
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187455
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SURF1 cytochrome c oxidase assembly factor |
CMT4K, MC4DN1, SHY1 |
Curated: Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cerebellar ataxia, Charcot-marie-tooth disease, Craniofacial abnormalities, Cytochrome c oxidase deficiency, Dejerine-sottas disease, Dysarthria, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Intellectual developmental disorder, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Peroneal muscle atrophy, Roussy-levy syndrome, Leigh syndrome, due to cox iv deficiency
Unreviewed: Acquired Kyphoscoliosis, Anemia, Basal cell carcinoma, Basal ganglia disease, Brain stem neoplasms, Breast Cancer, Cardiomyopathy, Central Nervous System Demyelination, Cerebellar Ataxia, Charcot-Marie-Tooth Disease, Congenital kyphoscoliosis, Congestive Heart Failure, Cytochrome-C Oxidase Deficiency, Demyelinating diseases, Demyelinating neuropathy, Developmental Delay, Developmental regression, Dyskinetic Syndrome, Dysmorphic Features, Dysphagia, Encephalopathy, Epileptic encephalopathy, Facial dysmorphism, Hearing Loss, Horizontal nystagmus, Hyperinsulinism, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Hypocupremia, Lactic acidosis, Leigh Syndrome, Leigh Syndrome With Cardiomyopathy, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Mental retardation, Mitochondrial Diseases, Mitochondrial encephalopathy, Mood swings, Mouth disease, Movement Disorders, Necrotizing encephalomyelopathy, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy, Nonketotic Hyperglycinemia, Nystagmus, Optic Atrophy, Peripheral nervous system disease, Peripheral Neuropathy, Polyneuropathy, Ptosis, Pulmonary Stenosis, Renal agenesis, Renal dysplasia, Respiratory Failure, Retinal Diseases, Retinitis Pigmentosa, Seizures, Strabismus, Ventricular septal defect
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187456
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Surfeit 2 |
SURF-2 |
Curated: N/A
Unreviewed: N/A
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187457
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Surfeit 4 |
ERV29 |
Curated: Hoarding disorder, Ovarian cancer, Prostatic neoplasms
Unreviewed: Breast neoplasm, Neoplasms, Prostate cancer, Prostatic Neoplasms
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187458
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Surfeit 6 |
RRP14 |
Curated: Venous thromboembolism
Unreviewed: Breast neoplasm, Epithelial ovarian carcinoma, Ovarian cancer, Ovarian Epithelial carcinoma
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187459
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Surfeit 6 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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187460
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Sushi domain containing 1 |
- |
Curated: Amyotrophic lateral sclerosis, Brain aneurysm, Dental caries, Venous thromboembolism
Unreviewed: Intracranial Aneurysm
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