|
12221
|
|
|
REC8 meiotic recombination protein |
HR21spB, REC8L1, Rec8p |
|
|
12222
|
|
|
Ras converting CAAX endopeptidase 1 |
FACE2, RCE1A, RCE1B |
|
|
12223
|
|
|
Heterogeneous nuclear ribonucleoprotein D like |
HNRNP, HNRPDL, JKTBP, JKTBP2, LGMD1G, LGMDD3, laAUF1 |
|
|
12224
|
|
|
Cyclin D binding myb like transcription factor 1 |
DMP1, DMTF, MRUL, hDMP1 |
|
|
12225
|
|
|
Cadherin 1 |
Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM, UVO |
Adenocarcinoma, Anaplastic carcinoma, Benign neoplasm of stomach, Urinary bladder cancer, Bladder neoplasm, Blepharocheilodontic syndrome, Breast cancer, Invasive duct and lobular carcinoma, Mammary neoplasms, Breast carcinoma, Hereditary cancer syndrome, Carcinoma, Cleft palate and bilateral cleft lip, Clinodactyly, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital euryblepharon, Ductal carcinoma, Dysgerminoma, Endometrial neoplasms, Endometrial carcinoma, Gastric cancer, Gastritis, Hearing loss, Hereditary breast cancer, Hereditary nonpolyposis colorectal cancer, Hypodontia, Hypoplasia of the maxilla, Imperforate anus, Malignant melanoma of skin, Malnutrition, Marfan syndrome, Melanoma, Mesothelioma, Nasopharyngeal carcinoma, Neural tube defect, Oropharyngeal dysphagia, Otitis media, Ovarian neoplasm, Ovarian cancer, Ovarian carcinoma, Ovarian epithelial carcinoma, Ovarian papillary adenocarcinoma, Pancreatic neoplasm, Pancreatic cancer, Peg-shaped teeth, Prostatic neoplasms, Prostate cancer, Prostate cancer, hereditary, Salivary gland neoplasm, Malignant neoplasm of salivary gland, Stomach neoplasms, Stomach carcinoma, Syndactyly of fingers, Thyroid carcinoma, Ulcerative colitis, Velopharyngeal insufficiencyView all (43 more) |
|
12226
|
|
|
Solute carrier family 12 member 6 |
ACCPN, CMT2II, KCC3, KCC3A, KCC3B |
Acrocephaly, Agenesis of corpus callosum, Aqueductal stenosis, Barrett esophagus, Bipolar disorder, Brachycephaly, Camptodactyly of fingers, Corpus callosum agenesis neuronopathy, Corpus callosum agenesis-neuronopathy syndrome, Craniosynostosis, Developmental delay, Hemiplegia/hemiparesis, High palate, Hypoplasia of the maxilla, Macrotia, Mental retardation, Microcephaly, Motor delay, Myopia, Hypotonia, Nervous system diseases, Nystagmus, Peripheral axonal neuropathy, Polyneuropathy, Psychosis, Ptosis, Scoliosis, Sensory neuropathy, Strabismus, Syndactyly of the toesView all (15 more) |
|
12227
|
|
|
Potassium voltage-gated channel subfamily E regulatory subunit 2 |
ATFB4, LQT5, LQT6, MIRP1 |
|
|
12228
|
|
|
DiGeorge syndrome critical region gene 2 |
DGS-C, IDD, LAN, SEZ-12 |
Blepharophimosis, Conotruncal anomaly face syndrome, Digeorge syndrome, Dwarfism, Mental retardation, Microcephaly, Mood swings, Paranoia, Pierre-robin syndrome, Posterior embryotoxon, Pulmonary dysgenesis, Schizophrenia, Shprintzen syndrome, Specific learning disorder, Velopharyngeal insufficiency, Ventricular septal defectView all (1 more) |
|
12229
|
|
|
Synthesis of cytochrome C oxidase 2 |
CEMCOX1, ECGF1, Gliostatin, MC4DN2, MYP6, PD-ECGF, SCO1L, TP, TYMP, TdRPase |
Anemia, Cardioencephalomyopathy, Cardiomyopathy, Central nervous system inborn metabolic diseases, Charcot-marie-tooth disease, Congestive heart failure, Cytochrome-c oxidase deficiency, Developmental delay, Developmental regression, Dysarthria, Dyskinetic syndrome, Dysphagia, Exotropia, Fatal cytochrome c oxidase deficiency, Hypertrichosis, Hypertrophic cardiomyopathy, Leigh syndrome, Leigh syndrome with cardiomyopathy, Leukodystrophy, Limb muscle atrophy, Mental retardation, Mitochondrial diseases, Mitochondrial dna depletion syndrome, Mitochondrial encephalomyopathy, Motor delay, Myocardial diseases, Myopia, Necrotizing encephalomyelopathy, Nervous system diseases, Nystagmus, Optic atrophy, Polyneuropathy, Ptosis, Pulmonary stenosis, Rare isolated myopia, Renal agenesis, Renal dysplasia, Respiratory failure, Retinal diseasesView all (24 more) |
