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 15 of 33)

Gene UniProt Protein Type Disease
IL10RA Q13651 non-pleiotropic Inflammatory bowel disease 28 (IBD28) [MIM:613148]
IL11RA Q14626 non-pleiotropic Craniosynostosis and dental anomalies (CRSDA) [MIM:614188]
IL12RB1 P42701 non-pleiotropic Mendelian susceptibility to mycobacterial disease (MSMD) [MIM:209950]
IL17F Q96PD4 non-pleiotropic Candidiasis, familial, 6 (CANDF6) [MIM:613956]
IL17RD Q8NFM7 non-pleiotropic Hypogonadotropic hypogonadism 18 with or without anosmia (HH18) [MIM:615267]
IL31RA Q8NI17 non-pleiotropic Amyloidosis, primary localized cutaneous, 2 (PLCA2) [MIM:613955]
IL36RN Q9UBH0 non-pleiotropic Psoriasis generalized pustular (PSORP) [MIM:614204]
ILDR1 Q86SU0 non-pleiotropic Deafness, autosomal recessive, 42 (DFNB42) [MIM:609646]
IMPAD1 Q9NX62 non-pleiotropic Chondrodysplasia with joint dislocations, GPAPP type (CDP-GPAPP) [MIM:614078]
ING1 Q9UK53 non-pleiotropic Squamous cell carcinoma of the head and neck (HNSCC) [MIM:275355]
ING3 Q9NXR8 non-pleiotropic Squamous cell carcinoma of the head and neck (HNSCC) [MIM:275355]
INPPL1 O15357 non-pleiotropic Opsismodysplasia (OPSMD) [MIM:258480]
INS P01308 pleiotropic Hyperproinsulinemia, familial (FHPRI) [MIM:176730]
Maturity-onset diabetes of the young 10 (MODY10) [MIM:613370]
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176]
Diabetes mellitus, insulin-dependent, 2 (IDDM2) [MIM:125852]
INSL3 P51460 non-pleiotropic Cryptorchidism (CRYPTO) [MIM:219050]
INSR P06213 pleiotropic Rabson-Mendenhall syndrome (RMS) [MIM:262190]
Leprechaunism (LEPRCH) [MIM:246200]
Insulin-resistant diabetes mellitus with acanthosis nigricans type A (IRAN type A) [MIM:610549]
Diabetes mellitus, non-insulin-dependent (NIDDM) [MIM:125853]
Familial hyperinsulinemic hypoglycemia 5 (HHF5) [MIM:609968]
INVS Q9Y283 non-pleiotropic Nephronophthisis 2 (NPHP2) [MIM:602088]
IQSEC2 Q5JU85 non-pleiotropic Mental retardation, X-linked 1 (MRX1) [MIM:309530]
IRF6 O14896 pleiotropic Van der Woude syndrome 1 (VWS1) [MIM:119300]
Popliteal pterygium syndrome (PPS) [MIM:119500]
Non-syndromic orofacial cleft 6 (OFC6) [MIM:608864]
IRS1 P35568 non-pleiotropic Diabetes mellitus, non-insulin-dependent (NIDDM) [MIM:125853]
IRX5 P78411 non-pleiotropic Hamamy syndrome (HMMS) [MIM:611174]
ISPD A4D126 non-pleiotropic Muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A7 (MDDGA7) [MIM:614643]
ITGA3 P26006 non-pleiotropic Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital (ILNEB) [MIM:614748]
ITGA8 P53708 non-pleiotropic Renal hypodysplasia/aplasia 1 (RHDA1) [MIM:191830]
ITGB2 P05107 non-pleiotropic Leukocyte adhesion deficiency 1 (LAD1) [MIM:116920]
ITK Q08881 non-pleiotropic Lymphoproliferative syndrome 1 (LPFS1) [MIM:613011]
ITPA Q9BY32 non-pleiotropic Inosine triphosphate pyrophosphohydrolase deficiency (ITPAD) [MIM:613850]
IVD P26440 non-pleiotropic Isovaleric acidemia (IVA) [MIM:243500]
IYD Q6PHW0 non-pleiotropic Thyroid dyshormonogenesis 4 (TDH4) [MIM:274800]
JAG1 P78504 pleiotropic Alagille syndrome 1 (ALGS1) [MIM:118450]
Tetralogy of Fallot (TOF) [MIM:187500]
JAK2 O60674 pleiotropic Leukemia, acute myelogenous (AML) [MIM:601626]
Polycythemia vera (PV) [MIM:263300]
Thrombocythemia 3 (THCYT3) [MIM:614521]
JAM3 Q9BX67 non-pleiotropic Hemorrhagic destruction of the brain with subependymal calcification and cataracts (HDBSCC) [MIM:613730]
JPH2 Q9BR39 non-pleiotropic Cardiomyopathy, familial hypertrophic 17 (CMH17) [MIM:613873]
KAL1 P23352 non-pleiotropic Hypogonadotropic hypogonadism 1 with or without anosmia (HH1) [MIM:308700]
KARS Q15046 pleiotropic Charcot-Marie-Tooth disease, recessive, intermediate type, B (CMTRIB) [MIM:613641]
Deafness, autosomal recessive, 89 (DFNB89) [MIM:613916]
KBTBD13 C9JR72 non-pleiotropic Nemaline myopathy 6 (NEM6) [MIM:609273]
KCNA1 Q09470 non-pleiotropic Episodic ataxia 1 (EA1) [MIM:160120]
Myokymia isolated 1 (MK1) [MIM:160120]
KCNC3 Q14003 non-pleiotropic Spinocerebellar ataxia 13 (SCA13) [MIM:605259]
KCND3 Q9UK17 non-pleiotropic Spinocerebellar ataxia 19 (SCA19) [MIM:607346]
KCNE2 Q9Y6J6 pleiotropic Long QT syndrome 6 (LQT6) [MIM:613693]
Atrial fibrillation, familial, 4 (ATFB4) [MIM:611493]
KCNE3 Q9Y6H6 non-pleiotropic Brugada syndrome 6 (BRGDA6) [MIM:613119]
KCNJ1 P48048 non-pleiotropic Bartter syndrome 2 (BS2) [MIM:241200]
KCNJ11 Q14654 pleiotropic Familial hyperinsulinemic hypoglycemia 2 (HHF2) [MIM:601820]
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176]
Transient neonatal diabetes mellitus 3 (TNDM3) [MIM:610582]
KCNJ18 B7U540 non-pleiotropic Thyrotoxic periodic paralysis 2 (TTPP2) [MIM:613239]
KCNJ2 P63252 pleiotropic Long QT syndrome 7 (LQT7) [MIM:170390]
Short QT syndrome 3 (SQT3) [MIM:609622]
Atrial fibrillation, familial, 9 (ATFB9) [MIM:613980]
KCNJ5 P48544 pleiotropic Long QT syndrome 13 (LQT13) [MIM:613485]
Familial hyperaldosteronism 3 (FH3) [MIM:613677]
KCNJ8 Q15842 non-pleiotropic Sudden infant death syndrome (SIDS) [MIM:272120]
KCNK3 O14649 non-pleiotropic Pulmonary hypertension, primary, 4 (PPH4) [MIM:615344]
KCNK9 Q9NPC2 non-pleiotropic Birk-Barel mental retardation dysmorphism syndrome (BIBAS) [MIM:612292]
KCNMA1 Q12791 non-pleiotropic Generalized epilepsy and paroxysmal dyskinesia (GEPD) [MIM:609446]
KCNQ1 P51787 pleiotropic Long QT syndrome 1 (LQT1) [MIM:192500]
Jervell and Lange-Nielsen syndrome 1 (JLNS1) [MIM:220400]
Atrial fibrillation, familial, 3 (ATFB3) [MIM:607554]
Short QT syndrome 2 (SQT2) [MIM:609621]