|
921
|
|
|
Peroxiredoxin like 2A |
Adrx, C10orf58, FAM213A, PAMM |
|
|
922
|
|
|
PHD finger protein 6 |
BFLS, BORJ, CENP-31 |
Atrial septal defect, Blepharophimosis, Borjeson-forssman-lehmann syndrome, Cataract, Coffin-siris syndrome, Congenital cataract, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Dwarfism, Dysmorphic features, Gynecomastia, Hypogonadism, Mental retardation, Lymphoblastic leukemia, Macrocephaly, Macrotia, Microcephaly, Multiple congenital anomalies, Nervous system diseases, Nystagmus, Obesity, Oral cleft, Penile hypospadias, Penis agenesis, Ptosis, Scoliosis, Syndactyly of the toes, Talipes transversoplanusView all (14 more) |
|
923
|
|
|
PiggyBac transposable element derived 1 |
HUCEP-4, SCAND4, dJ874C20.4 |
|
|
924
|
|
|
Protein phosphatase 1 regulatory subunit 9B |
PPP1R6, PPP1R9, SPINO, Spn |
|
|
925
|
|
|
Phosphatidylinositol glycan anchor biosynthesis class O |
HPMRS2, hGPCR43 |
Accessory nipple, Autism, Brachycephaly, Clinodactyly, Colorectal cancer, Congenital epicanthus, Congenital pectus excavatum, Developmental delay, Esotropia, High palate, Hirschsprung disease, Hydronephrosis, Hyperopia, Hyperphosphatasia with mental retardation, Imperforate anus, Mental retardation, Malocclusion, Micrognathism, Oculomotor apraxia, Oculovestibuloauditory syndrome, Plagiocephaly, Scoliosis, SeizureView all (8 more) |
|
926
|
|
|
Pleckstrin homology domain containing A8 |
FAPP2 |
|
|
927
|
|
|
Pyridine nucleotide-disulphide oxidoreductase domain 2 |
C10orf33, FP3420, YUEF |
|
|
928
|
|
|
Phospholipid phosphatase 7 (inactive) |
C9orf67, NET39, PPAPDC3 |
|
|
929
|
|
|
PHD finger protein 5A |
INI, Rds3, SAP14b, SF3B7, SF3b14b, bK223H9.2 |
|
|
930
|
|
|
Protein tyrosine phosphatase non-receptor type 5 |
PTPSTEP, STEP, STEP61 |
|
