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