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 32 of 33)

Gene UniProt Protein Type Disease
VANGL2 Q9ULK5 non-pleiotropic Neural tube defects (NTD) [MIM:182940]
VAX1 Q5SQQ9 non-pleiotropic Microphthalmia, syndromic, 11 (MCOPS11) [MIM:614402]
VCP P55072 pleiotropic Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1 (IBMPFD1) [MIM:167320]
Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia (ALS14) [MIM:613954]
VHL P40337 pleiotropic Von Hippel-Lindau disease (VHLD) [MIM:193300]
Pheochromocytoma (PCC) [MIM:171300]
Erythrocytosis, familial, 2 (ECYT2) [MIM:263400]
Renal cell carcinoma (RCC) [MIM:144700]
VPS13A Q96RL7 non-pleiotropic Choreoacanthocytosis (CHAC) [MIM:200150]
VPS13B Q7Z7G8 non-pleiotropic Cohen syndrome (COH1) [MIM:216550]
VPS33B Q9H267 non-pleiotropic Arthrogryposis, renal dysfunction and cholestasis syndrome 1 (ARCS1) [MIM:208085]
VPS35 Q96QK1 non-pleiotropic Parkinson disease 17 (PARK17) [MIM:614203]
VPS37A Q8NEZ2 non-pleiotropic Spastic paraplegia 53, autosomal recessive (SPG53) [MIM:614898]
VPS45 Q9NRW7 non-pleiotropic Neutropenia, severe congenital 5, autosomal recessive (SCN5) [MIM:615285]
WAS P42768 pleiotropic Thrombocytopenia 1 (THC1) [MIM:313900]
Wiskott-Aldrich syndrome (WAS) [MIM:301000]
Neutropenia, severe congenital, X-linked (XLN) [MIM:300299]
WDR11 Q9BZH6 non-pleiotropic Hypogonadotropic hypogonadism 14 with or without anosmia (HH14) [MIM:614858]
WDR19 Q8NEZ3 pleiotropic Short-rib thoracic dysplasia 5 with or without polydactyly (SRTD5) [MIM:614376]
Nephronophthisis 13 (NPHP13) [MIM:614377]
Cranioectodermal dysplasia 4 (CED4) [MIM:614378]
WDR34 Q96EX3 non-pleiotropic Short-rib thoracic dysplasia 11 with or without polydactyly (SRTD11) [MIM:615633]
WDR36 Q8NI36 non-pleiotropic Glaucoma 1, open angle, G (GLC1G) [MIM:609887]
WDR60 Q8WVS4 non-pleiotropic Short-rib thoracic dysplasia 8 with or without polydactyly (SRTD8) [MIM:615503]
WDR62 O43379 non-pleiotropic Microcephaly 2, primary, autosomal recessive, with or without cortical malformations (MCPH2) [MIM:604317]
WDR65 Q96MR6 non-pleiotropic Van der Woude syndrome 2 (VWS2) [MIM:606713]
WDR81 Q562E7 non-pleiotropic Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 (CAMRQ2) [MIM:610185]
WFS1 O76024 pleiotropic Wolfram syndrome 1 (WFS1) [MIM:222300]
Wolfram-like syndrome autosomal dominant (WFSL) [MIM:614296]
Deafness, autosomal dominant, 6 (DFNA6) [MIM:600965]
Cataract 41 (CTRCT41) [MIM:116400]
WNK4 Q96J92 non-pleiotropic Pseudohypoaldosteronism 2B (PHA2B) [MIM:614491]
WNT10A Q9GZT5 pleiotropic Odonto-onycho-dermal dysplasia (OODD) [MIM:257980]
Tooth agenesis selective 4 (STHAG4) [MIM:150400]
WNT10B O00744 non-pleiotropic Split-hand/foot malformation 6 (SHFM6) [MIM:225300]
WNT5A P41221 non-pleiotropic Robinow syndrome autosomal dominant (DRS) [MIM:180700]
WNT7A O00755 pleiotropic Fuhrmann syndrome (FUHRS) [MIM:228930]
Limb pelvis hypoplasia aplasia syndrome (LPHAS) [MIM:276820]
WRAP53 Q9BUR4 non-pleiotropic Dyskeratosis congenita, autosomal recessive, 3 (DKCB3) [MIM:613988]
WRN Q14191 non-pleiotropic Werner syndrome (WRN) [MIM:277700]
WT1 P19544 pleiotropic Wilms tumor 1 (WT1) [MIM:194070]
Denys-Drash syndrome (DDS) [MIM:194080]
Meacham syndrome (MEACHS) [MIM:608978]
Nephrotic syndrome 4 (NPHS4) [MIM:256370]
Frasier syndrome (FS) [MIM:136680]
WWOX Q9NZC7 non-pleiotropic Spinocerebellar ataxia, autosomal recessive, 12 (SCAR12) [MIM:614322]
XDH P47989 non-pleiotropic Xanthinuria 1 (XU1) [MIM:278300]
XK P51811 non-pleiotropic McLeod syndrome (MLS) [MIM:300842]
XPA P23025 non-pleiotropic Xeroderma pigmentosum complementation group A (XP-A) [MIM:278700]
XPC Q01831 non-pleiotropic Xeroderma pigmentosum complementation group C (XP-C) [MIM:278720]
XPNPEP3 Q9NQH7 non-pleiotropic Nephronophthisis-like nephropathy 1 (NPHPL1) [MIM:613159]
YARS P54577 non-pleiotropic Charcot-Marie-Tooth disease, dominant, intermediate type, C (CMTDIC) [MIM:608323]
YARS2 Q9Y2Z4 non-pleiotropic Myopathy with lactic acidosis and sideroblastic anemia 2 (MLASA2) [MIM:613561]
ZAP70 P43403 non-pleiotropic Selective T-cell defect (STCD) [MIM:269840]
ZBTB16 Q05516 non-pleiotropic Skeletal defects, genital hypoplasia, and mental retardation (SGYMR) [MIM:612447]
ZBTB24 O43167 non-pleiotropic Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2) [MIM:614069]
ZC4H2 Q9NQZ6 non-pleiotropic Wieacker-Wolf syndrome (WRWF) [MIM:314580]
ZDHHC9 Q9Y397 non-pleiotropic Mental retardation, X-linked, syndromic, ZDHHC9-related (MRXSZ) [MIM:300799]
ZEB2 O60315 non-pleiotropic Mowat-Wilson syndrome (MOWS) [MIM:235730]
ZFP57 Q9NU63 non-pleiotropic Transient neonatal diabetes mellitus 1 (TNDM1) [MIM:601410]
ZFYVE27 Q5T4F4 non-pleiotropic Spastic paraplegia 33, autosomal dominant (SPG33) [MIM:610244]
ZIC2 O95409 non-pleiotropic Holoprosencephaly 5 (HPE5) [MIM:609637]
ZMYND10 O75800 non-pleiotropic Ciliary dyskinesia, primary, 22 (CILD22) [MIM:615444]
ZNF141 Q15928 non-pleiotropic Polydactyly, postaxial A6 (PAPA6) [MIM:615226]
ZNF335 Q9H4Z2 non-pleiotropic Microcephaly 10, primary, autosomal recessive (MCPH10) [MIM:615095]
ZNF513 Q8N8E2 non-pleiotropic Retinitis pigmentosa 58 (RP58) [MIM:613617]
ZNF592 Q92610 non-pleiotropic Spinocerebellar ataxia, autosomal recessive, 5 (SCAR5) [MIM:606937]