|
381
|
|
|
Sorting nexin 24 |
PRO1284, SBBI31 |
|
|
382
|
|
|
Signal peptidase complex subunit 1 |
HSPC033, SPC1, SPC12, YJR010C-A |
|
|
383
|
|
|
Solute carrier family 43 member 3 |
EEG1, ENBT1, FOAP-13, PRO1659, SEEEG-1 |
|
|
384
|
|
|
SET domain containing 2, histone lysine methyltransferase |
HBP231, HIF-1, HIP-1, HSPC069, HYPB, KMT3A, LLS, MRD70, RAPAS, SET2, p231HBP |
Accessory kidney, Adenocarcinoma, Agenesis of corpus callosum, Anxiety disorder, Arnold-chiari malformation, Autism, Breast cancer, Mammary neoplasms, Breast carcinoma, Chromophobe carcinoma, Developmental dysplasia of the hip, Craniosynostosis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Dysmorphic features, Embryonal rhabdomyosarcoma, Frontal bossing, Hearing loss, Heart septal defects, High palate, Hypoglycemia, Hypospadias, Leukemia, Luscan-lumish syndrome, Lymphoblastic leukemia, Macrocephaly, Macrotia, Malignant mesothelioma, Malignant neoplasm, Cystosarcoma phyllodes, Malocclusion, Marfan syndrome, Mental retardation, Micrognathism, Multiple renal cysts, Nervous system neoplasms, Neurodevelopmental disorders, Obesity, Otitis media, Papillary renal carcinoma, Patent ductus arteriosus, Phyllodes tumor, Polycystic ovary syndrome, Precocious puberty, Prostatic neoplasms, Prostate cancer, Renal carcinoma, Sacrococcygeal teratoma, Scoliosis, Sotos` syndrome, Strabismus, Syringomyelia, Vesicoureteral refluxView all (40 more) |
|
385
|
|
|
Syntaxin binding protein 6 |
HSPC156, amisyn |
|
|
386
|
|
|
Solute carrier family 25 member 4 |
AAC1, ANT, ANT 1, ANT1, MTDPS12, MTDPS12A, PEO2, PEO3, PEOA2, T1 |
Anxiety disorder, Atrial fibrillation, Bipolar disorder, Cardiomyopathic mitochondrial dna depletion syndrome, Cardiomyopathy, Cataract, Central visual impairment, Cerebellar atrophy, Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome, Corneal dystrophy, Diabetes mellitus, Diabetic cardiomyopathy, Dysarthria, Dysmorphic features, Dysphagia, External ophthalmoplegia, Facial paralysis, Gastroesophageal reflux disease, Gastroparesis, Glaucoma, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypothyroidism, Impaired cognition, Ketosis, Left ventricular hypertrophy, Major affective disorder, Mental depression, Migraine, Mitochondrial diseases, Mitochondrial dna deletion syndrome, Mitochondrial myopathy, Myopathy, Myopia, Nocturia, Nystagmus, Osteoporosis, Peripheral axonal neuropathy, Progressive external ophthalmoplegia, Progressive external ophthalmoplegia with mitochondrial dna deletions, Ptosis, Sengers syndrome, Strabismus, Ventricular arrhythmiaView all (29 more) |
|
387
|
|
|
SAP30 binding protein |
HCNGP, HTRG, HTRP |
|
|
388
|
|
|
Sorting nexin 8 |
Mvp1 |
|
|
389
|
|
|
Sorting nexin 10 |
OPTB8 |
Anemia, Cranial nerve paralysis, Craniosynostosis, Facial paralysis, Frontal bossing, Hydrocephalus, Liver neoplasms, Liver cancer, Macrocephaly, Malignant osteopetrosis, Nystagmus, Opsoclonus, Optic atrophy, Osteopetrosis, Otitis media, Pulmonary arterial hypertension, RhinitisView all (2 more) |
|
390
|
|
|
Striatin 4 |
PPP2R6C, ZIN, zinedin |
|
