|
841
|
|
|
Praja ring finger ubiquitin ligase 1 |
PRAJA1, RNF70 |
|
|
842
|
|
|
Pyruvate kinase M1/2 pseudogene 1 |
- |
|
|
843
|
|
|
Phosphorylase kinase catalytic subunit gamma 1 pseudogene 2 |
- |
|
|
844
|
|
|
PIK3CD antisense RNA 1 |
C1orf200 |
|
|
845
|
|
|
Serine protease 56 |
MCOP6 |
|
|
846
|
|
|
Phospholipid phosphatase related 2 |
LPPR2, PRG4 |
|
|
847
|
|
|
Poly(ADP-ribose) polymerase family member 12 |
ARTD12, MST109, MSTP109, ZC3H1, ZC3HDC1 |
|
|
848
|
|
|
Purinergic receptor P2Y12 |
ADPG-R, BDPLT8, HORK3, P2T(AC), P2Y(12)R, P2Y(AC), P2Y(ADP), P2Y(cyc), P2Y12, SP1999 |
|
|
849
|
|
|
Porcupine O-acyltransferase |
DHOF, FODH, MG61, PORC, PPN |
Accessory nipple, Agenesis of corpus callosum, Alopecia, Aniridia, Arnold-chiari malformation, Brachydactyly, Congenital coloboma of iris, Congenital diaphragmatic hernia, Developmental dysplasia of the hip, Congenital exomphalos, Short clavicles, Congenital malrotation of intestine, Congenital omphalocele, Cryptorchidism, Dental enamel hypoplasia, Duodenal atresia, Dwarfism, Ectopia lentis, Focal dermal hypoplasia, Fundus coloboma, Gastroesophageal reflux disease, Giant cell tumor of bone, Hearing loss, Hiatal hernia, Horseshoe kidney, Hydrocephalus, Hydronephrosis, Hyperthyroxinemia, dysalbuminemic, Hypodontia, Hypoplasia of iris, Hypoplasia of nipple, Impaired cognition, Liver failure, Meningomyelocele, Mental retardation, Microcephaly, Microphthalmos, Multicystic renal dysplasia, Nail diseases, Nail dysplasia, Nail dystrophy, Nystagmus, Oligodontia, Optic atrophy, Osteopathia striata, Papilloma, Patent ductus arteriosus, Polydactyly, Polydactyly of toes, Retinal coloboma, Scoliosis, Spina bifida, Spina bifida occulta, Split hand foot deformity, Stenosis of external auditory canal, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Syndromic microphthalmia, Postaxial hand polydactyly, Ventricular septal defectView all (46 more) |
|
850
|
|
|
Pleckstrin homology and RhoGEF domain containing G2 |
ARHGEF42, CLG, CTB-60E11.4, LDAMD |
|
