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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UniProtID Disease Name

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


1602 items found (page 30 of 33)

Gene UniProt Protein Type Disease
TFR2 Q9UP52 non-pleiotropic Hemochromatosis 3 (HFE3) [MIM:604250]
TGFB2 P61812 non-pleiotropic Loeys-Dietz syndrome 4 (LDS4) [MIM:614816]
TGFB3 P10600 non-pleiotropic Rienhoff syndrome (RNHF) [MIM:615582]
TGFBR1 P36897 pleiotropic Loeys-Dietz syndrome 1 (LDS1) [MIM:609192]
Multiple self-healing squamous epithelioma (MSSE) [MIM:132800]
TGFBR2 P37173 pleiotropic Hereditary non-polyposis colorectal cancer 6 (HNPCC6) [MIM:614331]
Esophageal cancer (ESCR) [MIM:133239]
Loeys-Dietz syndrome 2 (LDS2) [MIM:610168]
TGIF1 Q15583 non-pleiotropic Holoprosencephaly 4 (HPE4) [MIM:142946]
TGM1 P22735 non-pleiotropic Ichthyosis, congenital, autosomal recessive 1 (ARCI1) [MIM:242300]
TGM5 O43548 non-pleiotropic Peeling skin syndrome, acral type (APSS) [MIM:609796]
TGM6 O95932 non-pleiotropic Spinocerebellar ataxia 35 (SCA35) [MIM:613908]
TH P07101 non-pleiotropic Segawa syndrome autosomal recessive (ARSEGS) [MIM:605407]
THAP1 Q9NVV9 non-pleiotropic Dystonia 6, torsion (DYT6) [MIM:602629]
THBD P07204 pleiotropic Hemolytic uremic syndrome atypical 6 (AHUS6) [MIM:612926]
Thrombophilia due to thrombomodulin defect (THPH12) [MIM:614486]
THOC6 Q86W42 non-pleiotropic Beaulieu-Boycott-Innes syndrome (BBIS) [MIM:613680]
THRB P10828 pleiotropic Generalized thyroid hormone resistance (GTHR) [MIM:188570]
Selective pituitary thyroid hormone resistance (PRTH) [MIM:145650]
TIA1 P31483 non-pleiotropic Welander distal myopathy (WDM) [MIM:604454]
TICAM1 Q8IUC6 non-pleiotropic Herpes simplex encephalitis 4 (HSE4) [MIM:614850]
TIMP3 P35625 non-pleiotropic Sorsby fundus dystrophy (SFD) [MIM:136900]
TJP2 Q9UDY2 non-pleiotropic Familial hypercholanemia (FHCA) [MIM:607748]
TK2 O00142 non-pleiotropic Mitochondrial DNA depletion syndrome 2 (MTDPS2) [MIM:609560]
TLL1 O43897 non-pleiotropic Atrial septal defect 6 (ASD6) [MIM:613087]
TLR3 O15455 non-pleiotropic Herpes simplex encephalitis 2 (HSE2) [MIM:613002]
TMEM138 Q9NPI0 non-pleiotropic Joubert syndrome 16 (JBTS16) [MIM:614465]
TMEM165 Q9HC07 non-pleiotropic Congenital disorder of glycosylation 2K (CDG2K) [MIM:614727]
TMEM43 Q9BTV4 pleiotropic Arrhythmogenic right ventricular dysplasia, familial, 5 (ARVD5) [MIM:604400]
Emery-Dreifuss muscular dystrophy 7, autosomal dominant (EDMD7) [MIM:614302]
TMEM5 Q9Y2B1 non-pleiotropic Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A10 (MDDGA10) [MIM:615041]
TMEM67 Q5HYA8 pleiotropic Meckel syndrome 3 (MKS3) [MIM:607361]
COACH syndrome (COACHS) [MIM:216360]
Joubert syndrome 6 (JBTS6) [MIM:610688]
Nephronophthisis 11 (NPHP11) [MIM:613550]
TMEM70 Q9BUB7 non-pleiotropic Mitochondrial complex V deficiency, nuclear 2 (MC5DN2) [MIM:614052]
TMIE Q8NEW7 non-pleiotropic Deafness, autosomal recessive, 6 (DFNB6) [MIM:600971]
TMPO P42166 non-pleiotropic Cardiomyopathy, dilated 1T (CMD1T) [MIM:613740]
TMPRSS6 Q8IU80 non-pleiotropic Iron-refractory iron deficiency anemia (IRIDA) [MIM:206200]
TNC P24821 non-pleiotropic Deafness, autosomal dominant, 56 (DFNA56) [MIM:615629]
TNFRSF4 P43489 non-pleiotropic Immunodeficiency 16 (IMD16) [MIM:615593]
TNFSF11 O14788 non-pleiotropic Osteopetrosis, autosomal recessive 2 (OPTB2) [MIM:259710]
TNNI2 P48788 non-pleiotropic Arthrogryposis, distal, 2B (DA2B) [MIM:601680]
TNNT3 P45378 non-pleiotropic Arthrogryposis, distal, 2B (DA2B) [MIM:601680]
TOR1A O14656 non-pleiotropic Dystonia 1, torsion, autosomal dominant (DYT1) [MIM:128100]
TP63 Q9H3D4 pleiotropic Split-hand/foot malformation 4 (SHFM4) [MIM:605289]
Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3) [MIM:604292]
Ectodermal dysplasia, Rapp-Hodgkin type (EDRH) [MIM:129400]
Acro-dermato-ungual-lacrimal-tooth syndrome (ADULT syndrome) [MIM:103285]
Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) [MIM:106260]
Non-syndromic orofacial cleft 8 (OFC8) [MIM:129400]
TPI1 P60174 non-pleiotropic Triosephosphate isomerase deficiency (TPID) [MIM:615512]
TPK1 Q9H3S4 non-pleiotropic Thiamine metabolism dysfunction syndrome 5, episodic encephalopathy type (THMD5) [MIM:614458]
TPM2 P07951 pleiotropic Nemaline myopathy 4 (NEM4) [MIM:609285]
Arthrogryposis, distal, 1A (DA1A) [MIM:108120]
Arthrogryposis, distal, 2B (DA2B) [MIM:601680]
Cap myopathy 2 (CAPM2) [MIM:609285]
TPMT P51580 non-pleiotropic Thiopurine S-methyltransferase deficiency (TPMT deficiency) [MIM:610460]
TPO P07202 non-pleiotropic Thyroid dyshormonogenesis 2A (TDH2A) [MIM:274500]
TPP1 O14773 pleiotropic Ceroid lipofuscinosis, neuronal, 2 (CLN2) [MIM:204500]
Spinocerebellar ataxia, autosomal recessive, 7 (SCAR7) [MIM:609270]
TRAF3 Q13114 non-pleiotropic Herpes simplex encephalitis 3 (HSE3) [MIM:614849]
TRAPPC11 Q7Z392 non-pleiotropic Limb-girdle muscular dystrophy 2S (LGMD2S) [MIM:615356]
TRAPPC2 P0DI81 non-pleiotropic Spondyloepiphyseal dysplasia tarda (SEDT) [MIM:313400]
TRDN Q13061 non-pleiotropic Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness (CPVT5) [MIM:615441]
TREM2 Q9NZC2 non-pleiotropic Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL) [MIM:221770]
TREX1 Q9NSU2 pleiotropic Aicardi-Goutieres syndrome 1 (AGS1) [MIM:225750]
Systemic lupus erythematosus (SLE) [MIM:152700]
Chilblain lupus 1 (CHBL1) [MIM:610448]
TRIM2 Q9C040 non-pleiotropic Charcot-Marie-Tooth disease 2R (CMT2R) [MIM:615490]