1181
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|
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Solute carrier family 24 member 5 |
JSX, NCKX5, OCA6, SHEP4 |
Curated: Eye neoplasms, Melanoma, Glaucoma, Oculocutaneous albinism, Open angle glaucoma, Pulmonary arterial hypertension, Scoliosis, Skin cancer, Skin disease, Skin neoplasms, Skin hair eye pigmentation variation
Unreviewed: Albinism, Color vision deficiency, Disorder Of Eye, Hypopigmentation Disorder, Kidney Disease, Kidney Failure, Medulloblastoma, Nystagmus, Ocular albinism, Ovarian neoplasm, Rufous oculocutaneous albinism, Squamous cell carcinoma
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1182
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|
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Solute carrier family 25 member 1 |
CIC, CMS23, CTP, D2L2AD, SEA, SLC20A3 |
Curated: Combined d-2- and l-2-hydroxyglutaric aciduria, Presynaptic congenital myasthenic syndrome, Congenital myasthenic syndrome, D-2-hydroxyglutaric aciduria, Mitochondrial disease, Myasthenic syndrome
Unreviewed: Acquired Kyphoscoliosis, Acute Myeloid Leukemia, Adrenocortical carcinoma, Agenesis Of Corpus Callosum, alpha Thalassemia, Anemia, Arthritis, Arthrogryposis multiplex congenita, Atopic dermatitis, Autism, Behcet disease, Behcet Syndrome, beta Thalassemia, Biliary Cirrhosis, Bladder carcinoma, Bladder Neoplasm, Blast phase chronic myelogenous leukemia, Brain disease, Breast Cancer, Breast Carcinoma, Bulbar palsy, Carcinoma, Cerebellar Hypoplasia, Cirrhosis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Congenital kyphoscoliosis, Congenital Pectus Carinatum, Corneal astigmatism, Coronary artery disease, Coronary Stenosis, Dermatitis, Developmental Delay, Developmental disability, Developmental dysplasia of the hip, DiGeorge Syndrome, Distal amyotrophy, Down Syndrome, Dysphagia, Eczema, Edema, End Stage Liver Disease, Epileptic encephalopathy, Esotropia, Fabry disease, Facioscapulohumeral Muscular Dystrophy, Fibromuscular Dysplasia, Frontometaphyseal Dysplasia, Gastroesophageal Reflux Disease, Gaucher Disease, Hearing Loss, Heart Diseases, Hemoglobin H Disease, Hemoglobinopathy, Hepatic Encephalopathy, Hepatocellular carcinoma, High palate, Hydrocephalus, Hydrops Fetalis, Hypochromic microcytic anemia, Hypogonadism, Hypoparathyroidism, Hypoplasia Of The Optic Nerve, Intellectual developmental disorder, Ischemic Stroke, Islet Cell Tumor, Kidney Cancer, Lamellar ichthyosis, Leukemia, Liver carcinoma, Liver Cirrhosis, Lung Cancer, Lung carcinoma, Lymphocytic Leukemia, Malignant Neoplasm, Megakaryocytic Leukemia, Mental retardation, Micrognathism, Motor delay, Moyamoya Disease, Mucolipidosis, Multiple Endocrine Neoplasia, Myasthenia Gravis, Myasthenic Syndrome, Myeloid leukemia, Myocardial Infarction, Neoplasms, Neuroblastoma, Nystagmus, Ovarian neoplasm, Polyneuropathy, Psoriasis, Ptosis, Renal Carcinoma, Rhinosinusitis With Nasal Polyps, Schizophrenia, Scleroderma, Seizures, Senile Plaques, Septicemia, Shprintzen Syndrome, Shprintzen-Goldberg Syndrome, Sickle cell anemia, Skin Lesion, Sleep Apnea, Spina Bifida, Stroke, Sudden episodic apnea, Thalassemia, Toxic Shock Syndrome, Triple Negative Breast Neoplasms, Urinary bladder cancer, Vascular Diseases, Ventricular septal defect
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1183
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|
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Solute carrier family 25 member 10 |
DIC, MTDPS19 |
Curated: Carcinoma, Dental caries, Hearing loss, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial dna depletion syndrome
Unreviewed: Anaplastic Carcinoma, Arthritis, Arthropathy, Congenital Chromosomal Disease, Congenital Thrombotic Thrombocytopenic Purpura, Diabetes mellitus, type 2, Disseminated Intravascular Coagulation, Epileptic encephalopathy, Hematological Disease, Hemolytic Uremic Syndrome, Inflammatory bowel disease, Leukemia, Liver carcinoma, Liver Fibrosis, Microangiopathic hemolytic anemia, Mitochondrial Complex Deficiency, Necrotizing Enterocolitis, Neoplasms, Neurodegenerative disorder, Neurodegenerative Disorders, Obesity, Ovarian neoplasm, Promyelocytic Leukemia, Purpura Fulminans, Pyruvate Carboxylase Deficiency Disease, Septicemia, Thrombophilia, Thrombotic Microangiopathies, Thrombotic thrombocytopenic purpura, Trichohepatoenteric Syndrome
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1184
|
|
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Solute carrier family 25 member 11 |
OGC, PGL6, PPGL6, SLC20A4 |
Curated: Metabolic syndrome, Pheochromocytoma/paraganglioma syndrome, Diabetes mellitus type 2
Unreviewed: Adrenal Gland Pheochromocytoma, Aniridia, Capillary Hemangioma Of Retina, Congestive Heart Failure, Cranial nerve compression, Episodic paroxysmal anxiety, Extra-Adrenal Pheochromocytoma, Glomerulonephritis, Glomerulosclerosis, Hearing Loss, Hepatocellular carcinoma, Hereditary Pheochromocytoma-Paraganglioma, Hypercalcemia, Hypertension, Hypertensive Retinopathy, Leiomyosarcoma, Liver Cancer, Liver carcinoma, Lung carcinoma, Lung Neoplasms, Malignant Neoplasm, Neoplasms, Pancreatic neoplasm, Panic Disorder, Paraganglioma, Paraganglioma of head and neck, Pulsatile Tinnitus, Renal Carcinoma, Renal cell carcinoma, Respiratory Distress Syndrome, Sinus Tachycardia, Vocal Cord Paralysis
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1185
|
|
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Solute carrier family 25 member 12 |
AGC1, ARALAR, DEE39, EIEE39 |
Curated: Rheumatoid arthritis, Asperger syndrome, Autism, Developmental and epileptic encephalopathy, Major depressive disorder, Mitochondrial disease, Schizophrenia, Amyotrophic lateral sclerosis, Diabetes mellitus type 2
Unreviewed: Arthritis, Atrophy, Autism spectrum disorder, Cerebral hypomyelination, Citrullinemia, Demyelinating diseases, Developmental Delay, Developmental disability, Diabetic foot, Epilepsy, Epileptic encephalopathy, Epileptic Encephalopathy With Global Cerebral Demyelination, Hepatocellular carcinoma, Hypersensitivity, Intellectual developmental disorder, Intervertebral Disc Degeneration, Lateral Sclerosis, Liver carcinoma, Mental retardation, Metachromatic leukodystrophy, Microcephaly, Motor neuron disease, Myopia, Neoplasms, Neurodegenerative disorder, Seizures
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1186
|
|
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Solute carrier family 25 member 13 |
ARALAR2, CITRIN, CTLN2, NICCD |
Curated: Citrin deficiency, Citrullinemia, Urea cycle disorder, Lung cancer, Osteoarthritis, Squamous cell carcinoma
Unreviewed: Anemia, Blood coagulation disorder, Cataract, Cholestasis, Cirrhosis, Citrin Deficiency, Cleft Lip With Or Without Cleft Palate, Colorectal Cancer, Colorectal neoplasm, Conjugated hyperbilirubinemia, Delayed menarche, Delirium, Delusions, Developmental Delay, Epileptic encephalopathy, Esophageal atresia, Fatty Liver, Glioblastoma, Glioma, Hallucinations, Hepatic Encephalopathy, Hepatocellular carcinoma, Hyperammonemia, Hyperbilirubinemia, Hypercholesterolemia, Hyperferritinemia, Hyperlysinemia, Hypoalbuminemia, Hypoglycemia, Hypoproteinemia, Inborn Errors Of Metabolism, Intellectual developmental disorder, Intrahepatic Cholestasis, Jaundice, Ketonuria, Liver carcinoma, Liver failure, Liver Fibrosis, Manic Disorder, Melanoma, Metabolic Diseases, Methylmalonic acidemia, Neoplasms, Non-Alcoholic Fatty Liver Disease, Pancreatic Diseases, Pancreatitis, Physiologic Amenorrhea, Psychosis, Stomach neoplasms, Tyrosinemia
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1187
|
|
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Solute carrier family 25 member 14 |
BMCP1, UCP5 |
Curated: N/A
Unreviewed: Brain Infarction, Carotid artery stenosis, Cortical development malformation, Diabetes mellitus, Head and neck neoplasm, Hypertension, Multiple Sclerosis, Schizophrenia
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1188
|
|
|
Solute carrier family 25 member 14 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1189
|
|
|
Solute carrier family 25 member 15 |
D13S327, HHH, LNC-HC, ORC1, ORNT1 |
Curated: Amino acid metabolism disorder, Cardiac arrhythmia, Citrullinemia, Urea cycle disorder, Intellectual developmental disorder, ornithine translocase deficiency
Unreviewed: Anotia, Apraxia, Arrhythmogenic right ventricular cardiomyopathy, Blepharophimosis, Blood Coagulation Disorders, Breast aplasia, Breast hypoplasia, Breast neoplasm, Camptodactyly of fingers, Carcinogenesis, Cerebellar Ataxia, Cerebral cortical atrophy, Chorioretinal atrophy, Ciliopathies, Colorectal neoplasm, Congenital Camptodactyly, Congenital Clubfoot, Congenital Hypoplasia Of Penis, Congenital Microcephaly, Congenital Pectus Carinatum, Craniosynostosis, Cryptorchidism, Developmental Delay, Developmental disability, Dwarfism, Ear disease, Ear Diseases, Ear-Patella-Short Stature Syndrome, Ectodermal dysplasia, Encephalopathy, Epileptic encephalopathy, Epispadias, Esophageal squamous cell carcinoma, Fanconi anemia, Frontal bossing, Gastroesophageal Reflux Disease, Glioblastoma, Growth disorder, Hepatocellular carcinoma, High palate, Hyperammonemia, Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, Hypertrophy Of Clitoris, Hypoplasia of the maxilla, Hypospadias, Impaired Cognition, Inflammatory Bowel Disease, Leukemia, Liver carcinoma, Liver failure, Liver neoplasm, Mandibular aplasia, Meier-Gorlin Syndrome, Melanoma, Mental retardation, Microcephaly, Microdontia, Micrognathism, Microlissencephaly, Microstomia, Microtia, Mulibrey nanism, MUNGAN SYNDROME, Myeloid leukemia, Myeloproliferative disorder, Myoclonic Seizures, Neoplasms, Ornithine Carbamoyltransferase Deficiency, Osteochondritis Dissecans, Pancreatic neoplasm, Penis Agenesis, Pituitary dwarfism, Posteriorly Rotated Ear, Prostatic neoplasm, Psoriasis, Renal cell carcinoma, Respiratory Failure, Seckel Syndrome, Spastic Paraplegia, Specific Learning Disorder, Squamous cell carcinoma, Stomach neoplasms, Strabismus, Subarachnoid hemorrhage, Submucosal cleft palate, Syndactyly of fingers, Triple negative breast cancer, Urinary bladder neoplasms
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1190
|
|
|
Solute carrier family 25 member 15 pseudogene 1 |
SLC25A15P, SLC25A15PY1 |
Curated: N/A
Unreviewed: N/A
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