|
351
|
|
|
Protocadherin 7 |
BH-Pcdh, BHPCDH, PPP1R120 |
|
|
352
|
|
|
Protocadherin 8 |
ARCADLIN, PAPC |
|
|
353
|
|
|
Protocadherin 9 |
- |
|
|
354
|
|
|
Presequence translocase associated motor 16 |
CGI-136, MAGMAS, SMDMDM, TIM16, TIMM16 |
Chondrodysplasia punctata, Developmental delay, Dwarfism, Frontal bossing, Hypertension, Micromelia, Microtia, Nephronophthisis, Pulmonary arterial hypertension, Sacral dysgenesis, Spondylometaphyseal dysplasia, Strudwick syndrome |
|
355
|
|
|
Phosphoenolpyruvate carboxykinase 1 |
PCKDC, PEPCK-C, PEPCK1, PEPCKC |
Celiac disease, Cerebral atrophy, Congestive heart failure, Developmental delay, Fatty liver, Heart failure, Hepatic encephalopathy, Hypoglycemia, Ketonuria, Liver carcinoma, Liver failure, Myocardial infarction, Obesity, Optic atrophy, Phosphoenolpyruvate carboxykinase deficiency, Renal steatosis, SchizophreniaView all (2 more) |
|
356
|
|
|
Phosphoenolpyruvate carboxykinase 2, mitochondrial |
PEPCK, PEPCK-M, PEPCK2, mtPCK2 |
|
|
357
|
|
|
Pericentriolar material 1 |
PTC4, RET/PCM-1 |
|
|
358
|
|
|
RNA polymerase I and III subunit D |
AC19, POLR1C, RPA16, RPA9, RPAC2, RPC16, RPO1-3, TCS2 |
Blepharospasm, Brachycephaly, Cataract, Choanal atresia, Congenital cerebral hernia, Congenital coloboma of iris, Congenital hypoplasia of penis, Congenital hypoplasia of thymus, Congenital ocular coloboma, Cryptorchidism, Developmental delay, Dysphasia, Enchondromatosis, Fistula of branchial cleft, Frontal bossing, Glossoptosis, Hearing loss, High palate, Hypoplasia of the maxilla, Leukemia, Lung adenocarcinoma, Macrostomia, Mandibulofacial dysostosis, Micrognathism, Microphthalmos, Microstomia, Microtia, Osteochondrodysplasia, Patent ductus arteriosus, Skeletal dysplasia, Strabismus, Thyroid hypoplasia, Treacher collins syndromeView all (18 more) |
|
359
|
|
|
Plasmolipin |
PMLP, TM4SF11 |
|
|
360
|
|
|
Protein-L-isoaspartate (D-aspartate) O-methyltransferase |
PIMT |
|
