1211
|
|
|
Solute carrier family 25 member 22 |
DEE3, EIEE3, GC-1, GC1, NET44 |
Curated: Developmental and epileptic encephalopathy, Developmental delay, Myoclonic encephalopathy, Epilepsy of infancy with migrating focal seizures, Malignant migrating partial seizures of infancy, genetic developmental and epileptic encephalopathy
Unreviewed: Absence epilepsy, Autism, Benign neonatal epilepsy, Cerebellar atrophy, Cerebral Atrophy, Choreoathetosis, Clonic Seizures, Colorectal Cancer, Colorectal neoplasm, Congenital Exomphalos, Cystic fibrosis, Developmental Delay, Developmental disability, Developmental regression, Dyskinetic Syndrome, Dysphagia, Dyssomnia, Epilepsy, Epileptic encephalopathy, Episodic Ataxia, Eyelid myoclonias, Febrile seizures, Focal Seizures, Focal Tonic Seizures, Gallbladder cancer, Hyperprolinemia, Hypoplasia Of Corpus Callosum, Hypotonia, Hypotonic seizures, Leber congenital amaurosis, Major depressive disorder, Malignant Neoplasm, Mental retardation, Microcephaly, Migrating Partial Seizures In Infancy, Myoclonic Encephalopathy, Myoclonic Epilepsy, Myoclonic Seizures, Neoplasms, Osteosarcoma, Pachygyria, Penis Agenesis, Precocious puberty, Renal dysplasia, Seizure, Seizures, Sleep Disorders, Spasms X-Linked, Strabismus, Ureterocele, Ventricular septal defect, West Syndrome
|
1212
|
|
|
Solute carrier family 25 member 23 |
APC2, MCSC2, SCAMC3, SCaMC-3 |
Curated: N/A
Unreviewed: Accessory Kidney, Alzheimer disease, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Capillary infantile hemangioma, Carcinogenesis, Carcinoma, Cardiovascular Abnormalities, Colitis, Colon Carcinoma, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Cortical development malformation, Craniosynostosis, Crohn disease, Cryptorchidism, Developmental Delay, Developmental dysplasia of the hip, Dolichocephaly, Epilepsy, Esophageal Carcinoma, Esophagus Neoplasm, Frontal bossing, Glioblastoma, Glioma, Granulosa Cell Tumor, Hearing Loss, Heart Septal Defects, High palate, Huntington Disease, Hypoglycemia, Hypospadias, Inflammatory Bowel Disease, Intellectual developmental disorder, Lissencephaly, Lung adenocarcinoma, Lung carcinoma, Lymphatic metastasis, Macrocephaly, Macrotia, Malignant Neoplasm, Malocclusion, Mammary Neoplasms, Marfan Syndrome, Mental retardation, Micrognathism, Multiple myeloma, Multiple polyposis syndrome, Multiple renal cysts, Neoplasms, Nervous System Neoplasms, Obesity, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Patent ductus arteriosus, Periventricular nodular heterotopia, Pineal Gland Neoplasm, Precocious puberty, Prostate cancer, Prostatic neoplasm, Renal cell carcinoma, Retinoblastoma, Sacrococcygeal teratoma, Scoliosis, Sotos` Syndrome, Strabismus, Subfertility, Ulcerative colitis, Urogenital Abnormalities, Vesicoureteral Reflux
|
1213
|
|
|
Solute carrier family 25 member 24 |
APC1, SCAMC-1, SCAMC1 |
Curated: Crohn disease, Dementia, Dental caries, Desbuquois syndrome, Eosinophilia, Heart failure, Inflammatory bowel disease, Ulcerative colitis, fontaine progeroid syndrome
Unreviewed: Abnormal dermatoglyphic pattern, Acrocephaly, Aortic Aneurysm, Astigmatism, Atrial Septal Defect, Bicuspid aortic valve, Bone disease, Brachycephaly, Breast Cancer, Breast Carcinoma, Breast neoplasm, Central Nervous System Neoplasms, Cerebellar Hypoplasia, Colorectal Cancer, Colorectal neoplasm, Conduct disorder, Congenital Absent Nipple, Congenital craniofacial dysostosis, Congenital Epicanthus, Congenital Exomphalos, Congenital heart defects, Coronal craniosynostosis, Craniosynostosis, Cryptorchidism, Defect Of Skull Ossification, Dwarfism, Gastroesophageal Reflux Disease, Glioma, Gorlin Chaudhry Moss Syndrome, Hearing Loss, Hydrocephalus, Hyperopia, HYPERTRICHOSIS, Hypodontia, Hypoplasia Of Corpus Callosum, Hypoplasia Of Nipple, Hypoplasia of the maxilla, Intraductal noninfiltrating carcinoma, Left Ventricular Hypertrophy, Lipoatrophy, Lipodystrophy, Malocclusion, Mental retardation, Metabolic syndrome, Microcephaly, Microdontia, Micrognathism, Microphthalmos, Microstomia, Mitochondrial disease, Multiple polyposis syndrome, Nystagmus, Oligodontia, Osteonecrosis, Patent ductus arteriosus, Penis Agenesis, Periventricular Nodular Heterotopia, Petty Laxova Wiedemann Syndrome, Posteriorly Rotated Ear, Progeroid Syndrome, Proptosis, Pulmonary arterial hypertension, Pulmonary hypoplasia, Sclerocornea, Scoliosis, Shagreen patch, Strabismus, Syndactyly, Synophrys, Tricuspid Valve Insufficiency
|
1214
|
|
|
SLC25A24 pseudogene 1 |
- |
Curated: N/A
Unreviewed: Esophagus Neoplasm
|
1215
|
|
|
SLC25A24 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1216
|
|
|
Solute carrier family 25 member 25 |
MCSC, PCSCL, SCAMC-2, SCAMC2 |
Curated: Autism, Nephrolithiasis, Myopia
Unreviewed: Asthma, Colorectal neoplasm, Diabetes mellitus, type 1, Eosinophilia, Melanoma
|
1217
|
|
|
SLC25A25 antisense RNA 1 |
HRCEG |
Curated: N/A
Unreviewed: Colorectal Cancer, Neoplasms
|
1218
|
|
|
Solute carrier family 25 member 26 |
COXPD28, SAMC |
Curated: Appendicitis, Atrial fibrillation, Binge eating disorder, Bipolar disorder, Kidney disease, Colorectal adenoma, Colorectal cancer, Combined oxidative phosphorylation deficiency, Hyperuricemia, Lymphoid leukemia, Mitochondrial disease, Pulmonary hypertension, Sarcoidosis, Scoliosis, Diabetes mellitus type 2
Unreviewed: Atrial Fibrillation, Bipolar Disorder, Bulimia, Cardiopulmonary Failure, Chronic obstructive pulmonary disease, Colonic Neoplasms, Colorectal Cancer, Colorectal Neoplasms, Combined Oxidative Phosphorylation Deficiency, Congestive Heart Failure, Developmental Delay, Edema, Kidney Failure, Respiratory Failure, Uterine neoplasm
|
1219
|
|
|
Solute carrier family 25 member 27 |
UCP4 |
Curated: Autoimmune thyroid disease, Graves disease, Hashimoto disease, Schizophrenia
Unreviewed: Alzheimer disease, Arthritis, Autoimmune Thyroiditis, Breast Carcinoma, Frontotemporal dementia, Graves Disease, Hashimoto Disease, Lung neoplasms, Mitochondrial complex deficiency, Multiple Sclerosis, Neoplasms, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Parkinson disease, Pica
|
1220
|
|
|
Solute carrier family 25 member 28 |
MFRN2, MRS3/4, MRS4L, NPD016 |
Curated: Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Colorectal adenoma, Colorectal cancer, Common variable immunodeficiency, Crohn disease, Diverticular disease, Glomerulonephritis, Hypothyroidism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Major depressive disorder, Psoriasis, Rheumatoid arthritis, Systemic lupus erythematosus, Diabetes mellitus type 1, Ulcerative colitis
Unreviewed: Glioma, Hepatocellular carcinoma, Huntington Disease, Mitochondrial disease, Parkinson disease, Squamous cell carcinoma
|