|
2391
|
|
|
Protein phosphatase, Mg2+/Mn2+ dependent 1K |
BCKDH, BDP, MSUDMV, PP2Ckappa, PP2Cm, PTMP, UG0882E07 |
|
|
2392
|
|
|
Adrenoceptor beta 1 |
ADRB1R, B1AR, BETA1AR, FNSS2, RHR |
Cardiomyopathy, Cardiovascular diseases, Congestive heart failure, Diabetes mellitus, Gastric cancer, Heart failure, Hyperemia, Hypertension, Mental depression, Mood disorder, Myocardial infarction, Myocardial ischemia, Obesity, Stomach neoplasms |
|
2393
|
|
|
RasGEF domain family member 1B |
GPIG4 |
|
|
2394
|
|
|
DAB2 interacting protein |
AF9Q34, AIP-1, AIP1, DIP1/2 |
|
|
2395
|
|
|
Solute carrier family 38 member 9 |
SNAT9, URLC11 |
|
|
2396
|
|
|
Solute carrier family 36 member 2 |
PAT2, TRAMD1 |
|
|
2397
|
|
|
CREB3 regulatory factor |
C5orf41, LRF |
|
|
2398
|
|
|
Centrosomal protein 120 |
CCDC100, JBTS31, SRTD13 |
Agenesis of corpus callosum, Ambiguous genitalia, Asphyxiating thoracic dystrophy, Atrial septal defect, Brachydactyly, Cerebellar hypoplasia, Cerebellar vermis agenesis, Congenital cerebral hernia, Congenital coloboma of iris, Congenital omphalocele, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Dextrocardia, Dwarfism, Foot polydactyly, Fundus coloboma, Hirschsprung disease, Hydrocephalus, Hypoplasia of corpus callosum, Impaired cognition, Imperforate anus, Jeune syndrome, Jeune thoracic dystrophy, Joubert syndrome, Joubert syndrome with ocular defect, Kidney disease, Macrocephaly, Macrotia, Majewski syndrome, Mental retardation, Micromelia, Microphthalmos, Multiple myeloma, Neck webbing, Nephronophthisis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Osteochondrodysplasia, Patent ductus arteriosus, Polydactyly, Polydactyly of toes, Polymicrogyria, Postaxial hand polydactyly, Ptosis, Pulmonary hypoplasia, Radial polydactyly, Renal cyst, Renal hypoplasia, Renal insufficiency, Retinal coloboma, Retinal dystrophy, Rhizomelia, Scoliosis, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia with or without polydactyly, Situs inversus, Skeletal dysplasia, Strabismus, Syndactyly of the toes, Ventricular septal defectView all (48 more) |
|
2399
|
|
|
Solute carrier family 25 member 48 |
- |
|
|
2400
|
|
|
Transmembrane protein 161B |
FLB3342, PRO1313 |
|
