|
211
|
|
|
Protein O-fucosyltransferase 1 |
DDD2, FUT12, O-FUT, O-Fuc-T, O-FucT-1, OFUCT1 |
|
|
212
|
|
|
PRAME nuclear receptor transcriptional regulator |
CT130, MAPE, OIP-4, OIP4 |
Chromophobe carcinoma, Head and neck neoplasms, Head neoplasms, Neck cancer, Neoplasm of head, Leukemia, Lung carcinoma, Head and neck cancer, Medulloblastoma, Medullomyoblastoma, Melanoma, Multiple myeloma, Myeloid leukemia, Neck neoplasms, Papillary renal carcinoma, Renal carcinoma, Sarcoma, Upper aerodigestive tract neoplasmsView all (3 more) |
|
213
|
|
|
Phosphoinositide-3-kinase regulatory subunit 5 |
F730038I15Rik, FOAP-2, P101-PI3K, p101 |
Ataxia-oculomotor apraxia, Cerebellar atrophy, Choreoathetosis, Colorectal cancer, Dysarthria, Dysphagia, Hypercholesterolemia, Hypoalbuminemia, Hypothyroidism, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Polyneuropathy, Sensorimotor neuropathy, Spinocerebellar ataxia, Spinocerebellar ataxia, with axonal neuropathy, StrabismusView all (2 more) |
|
214
|
|
|
Phosphatidylinositol glycan anchor biosynthesis class N |
GPI-ETI, MCAHS, MCAHS1, MCD4, MDC4, PIG-N |
Agenesis of corpus callosum, Asymmetric crying face association, Atrial septal defect, Brachydactyly, Camptodactyly of fingers, Cerebellar atrophy, Cerebral atrophy, Cerebral cortical atrophy, Choreoathetosis, Congenital diaphragmatic hernia, Congenital megaureter, Congenital epicanthus, Pulmonary hypoplasia, Congenital malrotation of intestine, Congenital omphalocele, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Double ureter, Duodenal atresia, Dysmorphic features, Dysphagia, Ectopic anus, Esotropia, Frontal bossing, Fryns syndrome, Gastroesophageal reflux disease, Heart septal defects, High palate, Hirschsprung disease, Hydronephrosis, Hypoplasia of corpus callosum, Hypospadias, Imperforate anus, Lung adenocarcinoma, Macrocephaly, Macrostomia, Mental retardation, Micrognathism, Microphthalmos, Microstomia, Microtia, Movement disorders, Multicystic renal dysplasia, Multiple congenital anomalies-hypotonia-seizures syndrome, Nystagmus, Paget disease, Partial absence of cerebellar vermis, Patent ductus arteriosus, Patent foramen ovale, Peripheral pulmonary artery stenosis, Posteriorly rotated ear, Pulmonary arterial hypertension, Renal dysplasia, Synophrys, Testicular hydrocele, Tetralogy of fallot, Ventricular hypertrophy, Vertical nystagmus, Vesicoureteral refluxView all (45 more) |
|
215
|
|
|
Peptidyl arginine deiminase 4 |
PAD, PAD4, PADI5, PDI4, PDI5 |
|
|
216
|
|
|
Decaprenyl diphosphate synthase subunit 1 |
COQ1, COQ10D2, COQ1A, DPS, SPS, TPRT, TPT, TPT 1, hDPS1 |
|
|
217
|
|
|
Pleckstrin homology like domain family A member 3 |
TIH1 |
|
|
218
|
|
|
Phospholipase D family member 3 |
AD19, HU-K4, HUK4, SCA46 |
|
|
219
|
|
|
Phospholipase A2 group XV |
ACS, GXVPLA2, LLPL, LPLA2, LYPLA3 |
|
|
220
|
|
|
Protein kinase D3 |
EPK2, PKC-NU, PKD3, PRKCN, nPKC-NU |
|
