|
261
|
|
|
Pre-mRNA processing factor 19 |
NMP200, PRP19, PSO4, SNEV, UBOX4, hPSO4 |
|
|
262
|
|
|
Proprotein convertase subtilisin/kexin type 1 inhibitor |
BigLEN, PEN, PROSAAS, SAAS, SCG8, SgVIII |
|
|
263
|
|
|
Piccolo presynaptic cytomatrix protein |
ACZ, PCH3 |
Bipolar disorder, Brachycephaly, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral atrophy, Developmental delay, Dwarfism, Hypoplasia of corpus callosum, Macrotia, Mental depression, Hypotonia, Optic atrophy, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia, Proptosis, Schizoaffective disorderView all (1 more) |
|
264
|
|
|
POC1 centriolar protein B |
CORD20, PIX1, TUWD12, WDR51B |
|
|
265
|
|
|
Prospero homeobox 2 |
PROX-2 |
|
|
266
|
|
|
Phosphoglycolate phosphatase |
AUM, G3PP, PGPase |
|
|
267
|
|
|
Phosphatidylinositol glycan anchor biosynthesis class W |
Gwt1, HPMRS5 |
Accessory nipple, Autism, Brachycephaly, Clinodactyly, Congenital epicanthus, Congenital pectus excavatum, Developmental delay, Esotropia, Glycosylphosphatidylinositol deficiency, High palate, Hirschsprung disease, Hydronephrosis, Hypercoagulability syndrome, Hyperopia, Hyperphosphatasia with mental retardation, Mental retardation, Macroglossia, Malocclusion, Micrognathism, Oculomotor apraxia, Oculovestibuloauditory syndrome, Plagiocephaly, Scoliosis, SeizureView all (9 more) |
|
268
|
|
|
Protein phosphatase 1 regulatory subunit 37 |
LRRC68 |
|
|
269
|
|
|
Peptidylprolyl isomerase like 6 |
PPIase, RSPH12, bA425D10.6, dJ919F19.1 |
|
|
270
|
|
|
Patatin like domain 1, omega-hydroxyceramide transacylase |
ARCI10, dJ50J22.1 |
Alopecia, Congenital ichthyosis, Congenital nonbullous ichthyosiform erythroderma, Corneal erosion, Dwarfism, Ectropion, Exfoliative dermatitis, Hypohidrosis, Ichthyosis, Ichthyosis congenita, Ichthyosis with hypotrichosis, Keratitis, Palmoplantar keratoderma, Xeroderma |
