991
|
|
|
Proprotein convertase subtilisin/kexin type 7 |
LPC, PC7, PC8, SPC7 |
|
992
|
|
|
PTTG1 regulator of sister chromatid separation, securin |
EAP1, ECRAR, HPTTG, PTTG, TUTR1 |
|
993
|
|
|
2-phosphoxylose phosphatase 1 |
ACPL2, HEL124, XYLP |
|
994
|
|
|
PDZ and LIM domain 7 |
LMP1, LMP3 |
|
995
|
|
|
PR/SET domain 6 |
KMT8C, PDA3, PRISM |
|
996
|
|
|
Phosphotriesterase related |
HPHRP, RPR-1 |
|
997
|
|
|
Phosphatidylinositol glycan anchor biosynthesis class M |
GPI-MT-I |
|
998
|
|
|
Post-GPI attachment to proteins phospholipase 3 |
AGLA546, CAB2, PERLD1, PP1498, hCOS16 |
Accessory nipple, Asthma, Autism, Bipolar disorder, Brachycephaly, Clinodactyly, Congenital diaphragmatic hernia, Congenital epicanthus, Congenital pectus excavatum, Developmental delay, Drachtman weinblatt sitarz syndrome, Dysmorphic features, Esotropia, High palate, Hirschsprung disease, Hydronephrosis, Hyperopia, Hyperphosphatasia with mental retardation, Mental retardation, Malocclusion, Micrognathism, Movement disorders, Oculomotor apraxia, Oculovestibuloauditory syndrome, Plagiocephaly, Scoliosis, Seizure, UranostaphyloschisisView all (13 more) |
999
|
|
|
Phospholipase A2 activating protein |
DOA1, NDMSBA, PLA2P, PLAP |
Bulbar palsy, Cerebellar cortical atrophy, Cerebral cortical atrophy, Congenital pectus carinatum, Developmental delay, Dysphagia, Ectrodactyly, Epileptic encephalopathy, Foot polydactyly, Hearing loss, High palate, Hyperhidrosis palmaris et plantaris, Hypoplasia of corpus callosum, Impaired cognition, Ischemic stroke, Leukoencephalopathy, Lymphoproliferative disorder, Mental retardation, Microcephaly, Micrognathism, Neurodevelopmental disorders, Neurodevelopmental disorder with microcephaly, spasticity, and brain anomalies, Nystagmus, Optic atrophy, Posteriorly rotated ear, Psychosis, Schizophrenia, Seizure, Severe combined immunodeficiency disease, Split hand foot deformity, Postaxial hand polydactyly, Vertical talusView all (17 more) |
1000
|
|
|
Palmitoyl-protein thioesterase 2 |
C6orf8, G14, PPT-2 |
|