|
871
|
|
|
Prader-Willi region non-protein coding RNA 1 |
LOHAN1, NCRNA00198 |
Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Clinodactyly, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Pelvic organ prolapse, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorderView all (8 more) |
|
872
|
|
|
Pleckstrin homology and FYVE domain containing 1 |
APPD, LAPF, PHAFIN1, ZFYVE15 |
|
|
873
|
|
|
Proline rich coiled-coil 2A |
BAT2, D6S51, D6S51E, G2 |
Breast cancer, Development disorder, Diabetes mellitus, Hodgkin disease, Lupus erythematosus, Membranous glomerulonephritis, Mental depression, Multiple sclerosis, Myasthenia gravis, Rheumatoid arthritis, Schizophrenia, Takayasu arteritis, Ulcerative colitis |
|
874
|
|
|
Phospholipase A2 group VII |
LDL-PLA2, LP-PLA2, PAFAD, PAFAH |
|
|
875
|
|
|
PiggyBac transposable element derived 5 |
- |
|
|
876
|
|
|
Protein phosphatase 1 regulatory subunit 3B |
GL, PPP1R4, PTG |
|
|
877
|
|
|
Poly(ADP-ribose) polymerase family member 8 |
ARTD16, pART16 |
|
|
878
|
|
|
Phosphopantothenoylcysteine synthetase |
CMD2C |
|
|
879
|
|
|
Partner and localizer of BRCA2 |
BROVCA5, FANCN, PNCA3 |
Anal canal carcinoma, Anorexia, Aplastic anemia, Astigmatism, Atrial septal defect, Azoospermia, Bilateral malignant neoplasm, Bipolar disorder, Breast adenocarcinoma, Breast cancer, Mammary neoplasms, Breast carcinoma, Cafe-au-lait spot, Camptodactyly of fingers, Hereditary cancer syndrome, Carcinoma, Cataract, Choanal atresia, Cholestasis, Colonic neoplasms, Colorectal neoplasms, Colorectal cancer, Congenital arteriovenous malformation, Congenital atresia of colon, Congenital epicanthus, Congenital exomphalos, Congenital pectus excavatum, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Diabetes mellitus, Dolichocephaly, Dwarfism, Exocrine pancreatic insufficiency, Fanconi anemia, Frontal bossing, Hemangiosarcoma, Hereditary breast and ovarian cancer syndrome, Hereditary breast cancer, Hereditary nonpolyposis colorectal cancer, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypoplasia of thumb, Hypospadias, Imperforate anus, Intestinal pseudoobstruction, Leukemia, Leukopenia, Liver neoplasms, Marfan syndrome, Meckel diverticulum, Medulloblastoma, Melanoma, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Nasopharyngeal neoplasms, Nephroblastoma, Neuroendocrine tumor of pancreas, Nystagmus, Ductal carcinoma, Ovarian neoplasm, Ovarian cancer, Ovarian carcinoma, Ovarian epithelial carcinoma, Pancreatic adenocarcinoma, Pancreatic carcinoma, Pancreatic neoplasm, Pancreatic cancer, Pancytopenia, Patent ductus arteriosus, Penile hypospadias, Peritoneal carcinoma, Proptosis, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer, Ptosis, Renal insufficiency, Scoliosis, Spina bifida, Stomach carcinoma, Strabismus, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallot, Tracheoesophageal fistula, Tumor predisposition syndrome, Uranostaphyloschisis, Ureter duplex, Ventricular septal defectView all (85 more) |
|
880
|
|
|
Pseudopodium enriched atypical kinase 1 |
SGK269 |
|
