Protein List

Listed below are all the proteins used in our analysis. You can refine the list by using the panel below.
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Statistics

Found 257  pleiotropic proteins  (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).

pleiotropic

1602 items found (page 27 of 33)

Gene UniProt Protein Type Disease
SH2D1A O60880 non-pleiotropic Lymphoproliferative syndrome, X-linked, 1 (XLP1) [MIM:308240]
SH3BP2 P78314 non-pleiotropic Cherubism (CRBM) [MIM:118400]
SH3PXD2B A1X283 non-pleiotropic Frank-Ter Haar syndrome (FTHS) [MIM:249420]
SHOC2 Q9UQ13 non-pleiotropic Noonan syndrome-like disorder with loose anagen hair (NSLH) [MIM:607721]
SHOX O15266 pleiotropic Leri-Weill dyschondrosteosis (LWD) [MIM:127300]
Langer mesomelic dysplasia (LMD) [MIM:249700]
SHROOM4 Q9ULL8 non-pleiotropic Mental retardation, X-linked, syndromic, Stocco dos Santos type (SDSX) [MIM:300434]
SI P14410 non-pleiotropic Congenital sucrase-isomaltase deficiency (CSID) [MIM:222900]
SIAE Q9HAT2 non-pleiotropic Autoimmune disease 6 (AIS6) [MIM:613551]
SIGMAR1 Q99720 non-pleiotropic Amyotrophic lateral sclerosis 16, juvenile (ALS16) [MIM:614373]
SIX5 Q8N196 non-pleiotropic Branchiootorenal syndrome 2 (BOR2) [MIM:610896]
SIX6 O95475 non-pleiotropic Microphthalmia, isolated, with cataract, 2 (MCOPCT2) [MIM:212550]
SKIV2L Q15477 non-pleiotropic Trichohepatoenteric syndrome 2 (THES2) [MIM:614602]
SLC10A2 Q12908 non-pleiotropic Primary bile acid malabsorption (PBAM) [MIM:613291]
SLC11A2 P49281 non-pleiotropic Anemia, hypochromic microcytic, with iron overload 1 (AHMIO1) [MIM:206100]
SLC12A1 Q13621 non-pleiotropic Bartter syndrome 1 (BS1) [MIM:601678]
SLC12A3 P55017 non-pleiotropic Gitelman syndrome (GS) [MIM:263800]
SLC16A2 P36021 non-pleiotropic Monocarboxylate transporter 8 deficiency (MCT8 deficiency) [MIM:300523]
SLC17A8 Q8NDX2 non-pleiotropic Deafness, autosomal dominant, 25 (DFNA25) [MIM:605583]
SLC19A2 O60779 non-pleiotropic Thiamine-responsive megaloblastic anemia syndrome (TRMA) [MIM:249270]
SLC19A3 Q9BZV2 non-pleiotropic Thiamine metabolism dysfunction syndrome 2, biotin- or thiamine-responsive type (THMD2) [MIM:607483]
SLC1A3 P43003 non-pleiotropic Episodic ataxia 6 (EA6) [MIM:612656]
SLC20A2 Q08357 non-pleiotropic Basal ganglia calcification, idiopathic, 1 (IBGC1) [MIM:213600]
SLC22A12 Q96S37 non-pleiotropic Hypouricemia renal 1 (RHUC1) [MIM:220150]
SLC22A18 Q96BI1 non-pleiotropic Lung cancer (LNCR) [MIM:211980]
SLC22A5 O76082 non-pleiotropic Systemic primary carnitine deficiency (CDSP) [MIM:212140]
SLC25A1 P53007 non-pleiotropic Combined D-2- and L-2-hydroxyglutaric aciduria (D2L2AD) [MIM:615182]
SLC25A12 O75746 non-pleiotropic Global cerebral hypomyelination (GCHM) [MIM:612949]
SLC25A15 Q9Y619 non-pleiotropic Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (HHH syndrome) [MIM:238970]
SLC25A20 O43772 non-pleiotropic Carnitine-acylcarnitine translocase deficiency (CACTD) [MIM:212138]
SLC25A22 Q9H936 non-pleiotropic Epileptic encephalopathy, early infantile, 3 (EIEE3) [MIM:609304]
SLC25A3 Q00325 non-pleiotropic Mitochondrial phosphate carrier deficiency (MPCD) [MIM:610773]
SLC25A38 Q96DW6 non-pleiotropic Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive (PRARSA) [MIM:205950]
SLC26A3 P40879 non-pleiotropic Diarrhea 1, secretory chloride, congenital (DIAR1) [MIM:214700]
SLC26A4 O43511 pleiotropic Deafness, autosomal recessive, 4 (DFNB4) [MIM:600791]
Pendred syndrome (PDS) [MIM:274600]
SLC26A8 Q96RN1 non-pleiotropic Spermatogenic failure 3 (SPGF3) [MIM:606766]
SLC27A4 Q6P1M0 non-pleiotropic Ichthyosis prematurity syndrome (IPS) [MIM:608649]
SLC29A3 Q9BZD2 non-pleiotropic Histiocytosis-lymphadenopathy plus syndrome (HLAS) [MIM:602782]
SLC2A1 P11166 pleiotropic GLUT1 deficiency syndrome 1 (GLUT1DS1) [MIM:606777]
GLUT1 deficiency syndrome 2 (GLUT1DS2) [MIM:612126]
Dystonia 9 (DYT9) [MIM:601042]
Epilepsy, idiopathic generalized 12 (EIG12) [MIM:614847]
SLC2A10 O95528 non-pleiotropic Arterial tortuosity syndrome (ATS) [MIM:208050]
SLC2A2 P11168 non-pleiotropic Fanconi-Bickel syndrome (FBS) [MIM:227810]
SLC2A4 P14672 non-pleiotropic Diabetes mellitus, non-insulin-dependent (NIDDM) [MIM:125853]
SLC30A2 Q9BRI3 non-pleiotropic Zinc deficiency, transient neonatal (TNZD) [MIM:608118]
SLC34A3 Q8N130 non-pleiotropic Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) [MIM:241530]
SLC35A2 P78381 non-pleiotropic Congenital disorder of glycosylation 2M (CDG2M) [MIM:300896]
SLC35C1 Q96A29 non-pleiotropic Congenital disorder of glycosylation 2C (CDG2C) [MIM:266265]
SLC39A4 Q6P5W5 non-pleiotropic Acrodermatitis enteropathica, zinc-deficiency type (AEZ) [MIM:201100]
SLC3A1 Q07837 non-pleiotropic Cystinuria (CSNU) [MIM:220100]
SLC40A1 Q9NP59 non-pleiotropic Hemochromatosis 4 (HFE4) [MIM:606069]
SLC46A1 Q96NT5 non-pleiotropic Hereditary folate malabsorption (HFM) [MIM:229050]
SLC4A1 P02730 pleiotropic Spherocytosis 4 (SPH4) [MIM:612653]
Renal tubular acidosis, distal, autosomal dominant (AD-dRTA) [MIM:179800]
Renal tubular acidosis, distal, with hemolytic anemia (dRTA-HA) [MIM:611590]
Renal tubular acidosis, distal, with normal red cell morphology (dRTA-NRC) [MIM:611590]