|
1021
|
|
|
Pumilio RNA binding family member 1 |
HSPUM, NEDMSF, PUMH, PUMH1, PUML1, SCA47 |
|
|
1022
|
|
|
Phosphatase and actin regulator 2 |
C6orf56 |
|
|
1023
|
|
|
Protocadherin alpha 9 |
PCDH-ALPHA9 |
|
|
1024
|
|
|
PCNA clamp associated factor |
KIAA0101, L5, NS5ATP9, OEATC, OEATC-1, OEATC1, PAF, PAF15, p15(PAF), p15/PAF, p15PAF |
|
|
1025
|
|
|
Piezo type mechanosensitive ion channel component 1 (Er blood group) |
DHS, ER, FAM38A, LMPH3, LMPHM6, Mib |
Anemia, Congenital pectus excavatum, Dehydrated hereditary stomatocytosis, Dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema, Developmental delay, Gastroesophageal reflux disease, Hydrops fetalis, Hypothyroidism, Lymphatic malformation, Neck webbing, Scoliosis, Testicular hydrocele, Vulval varices, Xerocytosis |
|
1026
|
|
|
Phosphatidylserine synthase 1 |
LMHD, PSS1, PSSA |
Absence of septum pellucidum, Agenesis of corpus callosum, Elbow ankylosis, Brachydactyly, Choanal atresia, Cryptorchidism, Cutis laxa, Cutis marmorata, Dental enamel hypoplasia, Developmental delay, Dwarfism, Elbow flexion contracture, Epispadias, Facial paralysis, Frontal bossing, Hearing loss, Hernia, femoral, Hydrocephalus, Hypogonadism, Hypospadias, Lenz-majewski hyperostosis syndrome, Macrocephaly, Macrostomia, Macrotia, Malocclusion, Mental retardation, Microglossia, Micrognathism, Osteopetrosis, Ramer ladda syndrome, Scoliosis, Specific learning disorder, Submucosal cleft palate, Syndactyly, Syndactyly of fingersView all (20 more) |
|
1027
|
|
|
Pleckstrin homology and RUN domain containing M1 |
AP162, B2, OPTA3, OPTB6 |
|
|
1028
|
|
|
Proteasome 26S subunit, non-ATPase 6 |
Rpn7, S10, SGA-113M, p42A, p44S10 |
|
|
1029
|
|
|
Phospholipid phosphatase related 4 |
LPPR4, LPR4, PHP1, PRG-1, PRG1 |
|
|
1030
|
|
|
Poly(A) specific ribonuclease subunit PAN2 |
USP52 |
|
