3881
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Synaptotagmin like 5 |
slp5 |
Curated: Anorexia nervosa, Eating disorder, Erectile dysfunction, Prostate cancer
Unreviewed: Anorexia, Bulimia, Colorectal neoplasm
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3882
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|
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Synoviolin 1 |
DER3, HRD1 |
Curated: Crohn disease, Hypospadias, Inflammatory bowel disease, Osteoarthritis, Schizophrenia
Unreviewed: Alzheimer disease, Arthritis, Arthropathy, Atherosclerosis, Autism Spectrum Disorder, Autoimmune Diseases, Breast Cancer, Breast Carcinoma, Carcinoma, Charcot-Marie-Tooth Disease, Colon Carcinoma, Colonic Neoplasms, Congenital Chromosomal Disease, Diabetes, Diabetes Mellitus, Diabetic Nephropathy, DiGeorge Syndrome, Enteritis, Facial dysmorphism, Fatty Liver, Hepatoblastoma, Hepatocellular carcinoma, Kenny-Caffey Syndrome, Kidney Cancer, Limb-Girdle Muscular Dystrophy, Liver carcinoma, Liver Cirrhosis, Lung carcinoma, Lung neoplasms, Lymphocytic Leukemia, Lymphoma, Malignant Neoplasm, Metabolic Syndrome, Monocytic Leukemia, Multiple Sclerosis, Myelodysplastic Syndrome, Nasal polyposis, Neoplasms, Neuroblastoma, Neurodegenerative Disorders, Obesity, Osteoglophonic dwarfism, Parkinson disease, Prostatic neoplasm, Psoriasis, Psoriasis vulgaris, Renal Carcinoma, Renal cell carcinoma, Renal fibrosis, Rheumatoid arthritis, Rhinosinusitis With Nasal Polyps, Sarcoglycanopathies, Septicemia, Squamous cell carcinoma, Von Hippel-Lindau Syndrome, Wolfram Syndrome
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3883
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SUZ RNA binding domain containing 1 |
C1orf144 |
Curated: N/A
Unreviewed: Carcinoma, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Malignant Neoplasm, Neoplasms, Oligodendroglioma
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3884
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|
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SZRD1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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3885
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|
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SZT2 subunit of KICSTOR complex |
C1orf84, DEE18, EIEE18, KIAA0467, KICS1, SZT2A, SZT2B |
Curated: Alzheimer disease, Developmental and epileptic encephalopathy, Encephalocele, Generalized epilepsy, Rolandic epilepsy, Global developmental delay, Hypertension, Intellectual developmental disorder, Obesity, Parkinson disease, genetic developmental and epileptic encephalopathy
Unreviewed: Attention Deficit Hyperactivity Disorder, Autism, Brain disease, Cardiovascular Diseases, Cerebral Atrophy, Corpus callosum agenesis, Cryptorchidism, Developmental Delay, Developmental disability, Developmental regression, Dwarfism, Dyskinetic Syndrome, Dysmorphic Features, Epilepsy, Epileptic encephalopathy, Gastroesophageal Reflux Disease, Hypodontia, Leukoencephalopathy, Macrocephaly, Mental retardation, Microcephaly, Non-Specifi Epileptic Encephalopathy, Nystagmus, Optic Atrophy, Psychiatric disorders, Ptosis, Seizures, Status Epilepticus, Tuberous sclerosis complex
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3886
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SZT2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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