Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 2 of 33)
| Gene | UniProt | Protein Type | Disease |
|---|---|---|---|
| AGA | P20933 | non-pleiotropic | Aspartylglucosaminuria (AGU) [MIM:208400] |
| AGBL1 | Q96MI9 | non-pleiotropic | Corneal dystrophy, Fuchs endothelial, 8 (FECD8) [MIM:615523] |
| AGGF1 | Q8N302 | non-pleiotropic | Klippel-Trenaunay syndrome (KTS) [MIM:149000] |
| AGPAT2 | O15120 | non-pleiotropic | Congenital generalized lipodystrophy 1 (CGL1) [MIM:608594] |
| AGPS | O00116 | non-pleiotropic | Rhizomelic chondrodysplasia punctata 3 (RCDP3) [MIM:600121] |
| AGRN | O00468 | non-pleiotropic | Myasthenia, limb-girdle, familial (LGM) [MIM:254300] |
| AGXT | P21549 | non-pleiotropic | Hyperoxaluria primary 1 (HP1) [MIM:259900] |
| AHCY | P23526 | non-pleiotropic | Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD) [MIM:613752] |
| AHI1 | Q8N157 | non-pleiotropic | Joubert syndrome 3 (JBTS3) [MIM:608629] |
| AICDA | Q9GZX7 | non-pleiotropic | Immunodeficiency with hyper-IgM 2 (HIGM2) [MIM:605258] |
| AIRE | O43918 | non-pleiotropic | Autoimmune polyendocrine syndrome 1, with or without reversible metaphyseal dysplasia (APS1) [MIM:240300] |
| AK1 | P00568 | non-pleiotropic | Hemolytic anemia due to adenylate kinase deficiency (HAAKD) [MIM:612631] |
| AK2 | P54819 | non-pleiotropic | Reticular dysgenesis (RDYS) [MIM:267500] |
| AKR1C2 | P52895 | non-pleiotropic | 46,XY sex reversal 8 (SRXY8) [MIM:614279] |
| AKR1D1 | P51857 | non-pleiotropic | Congenital bile acid synthesis defect 2 (CBAS2) [MIM:235555] |
| AKT1 | P31749 | pleiotropic | Breast cancer (BC) [MIM:114480] Proteus syndrome (PROTEUSS) [MIM:176920] |
| AKT3 | Q9Y243 | non-pleiotropic | Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH) [MIM:603387] |
| ALB | P02768 | non-pleiotropic | Dysalbuminemic hyperthyroxinemia (DH) [MIM:103600] |
| ALDH18A1 | P54886 | non-pleiotropic | Cutis laxa, autosomal recessive, 3A (ARCL3A) [MIM:219150] |
| ALDH1A3 | P47895 | non-pleiotropic | Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
| ALDH3A2 | P51648 | non-pleiotropic | Sjoegren-Larsson syndrome (SLS) [MIM:270200] |
| ALDH4A1 | P30038 | non-pleiotropic | Hyperprolinemia 2 (HP-2) [MIM:239510] |
| ALDH5A1 | P51649 | non-pleiotropic | Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
| ALDH6A1 | Q02252 | non-pleiotropic | Methylmalonate semialdehyde dehydrogenase deficiency (MMSDHD) [MIM:614105] |
| ALDH7A1 | P49419 | non-pleiotropic | Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
| ALDOA | P04075 | non-pleiotropic | Glycogen storage disease 12 (GSD12) [MIM:611881] |
| ALDOB | P05062 | non-pleiotropic | Hereditary fructose intolerance (HFI) [MIM:229600] |
| ALG1 | Q9BT22 | non-pleiotropic | Congenital disorder of glycosylation 1K (CDG1K) [MIM:608540] |
| ALG11 | Q2TAA5 | non-pleiotropic | Congenital disorder of glycosylation 1P (CDG1P) [MIM:613661] |
| ALG12 | Q9BV10 | non-pleiotropic | Congenital disorder of glycosylation 1G (CDG1G) [MIM:607143] |
| ALG13 | Q9NP73 | non-pleiotropic | Congenital disorder of glycosylation 1S (CDG1S) [MIM:300884] |
| ALG3 | Q92685 | non-pleiotropic | Congenital disorder of glycosylation 1D (CDG1D) [MIM:601110] |
| ALG6 | Q9Y672 | non-pleiotropic | Congenital disorder of glycosylation 1C (CDG1C) [MIM:603147] |
| ALG8 | Q9BVK2 | non-pleiotropic | Congenital disorder of glycosylation 1H (CDG1H) [MIM:608104] |
| ALG9 | Q9H6U8 | non-pleiotropic | Congenital disorder of glycosylation 1L (CDG1L) [MIM:608776] |
| ALK | Q9UM73 | non-pleiotropic | Neuroblastoma 3 (NBLST3) [MIM:613014] |
| ALOX12B | O75342 | non-pleiotropic | Ichthyosis, congenital, autosomal recessive 2 (ARCI2) [MIM:242100] |
| ALOXE3 | Q9BYJ1 | non-pleiotropic | Ichthyosis, congenital, autosomal recessive 3 (ARCI3) [MIM:606545] |
| ALX3 | O95076 | non-pleiotropic | Frontonasal dysplasia 1 (FND1) [MIM:136760] |
| AMELX | Q99217 | non-pleiotropic | Amelogenesis imperfecta 1E (AI1E) [MIM:301200] |
| AMH | P03971 | non-pleiotropic | Persistent Muellerian duct syndrome 1 (PMDS1) [MIM:261550] |
| AMHR2 | Q16671 | non-pleiotropic | Persistent Muellerian duct syndrome 2 (PMDS2) [MIM:261550] |
| AMN | Q9BXJ7 | non-pleiotropic | Recessive hereditary megaloblastic anemia 1 (RH-MGA1) [MIM:261100] |
| AMPD1 | P23109 | non-pleiotropic | Myopathy due to myoadenylate deaminase deficiency (MMDD) [MIM:615511] |
| AMPD3 | Q01432 | non-pleiotropic | Adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE) [MIM:612874] |
| AMT | P48728 | non-pleiotropic | Non-ketotic hyperglycinemia (NKH) [MIM:605899] |
| ANG | P03950 | non-pleiotropic | Amyotrophic lateral sclerosis 9 (ALS9) [MIM:611895] |
| ANK1 | P16157 | non-pleiotropic | Spherocytosis 1 (SPH1) [MIM:182900] |
| ANKH | Q9HCJ1 | pleiotropic | Craniometaphyseal dysplasia, autosomal dominant (CMDD) [MIM:123000] Chondrocalcinosis 2 (CCAL2) [MIM:118600] |
| ANKRD1 | Q15327 | non-pleiotropic | Total anomalous pulmonary venous return (TAPVR) [MIM:106700] |