Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 20 of 33)
| Gene | UniProt | Protein Type | Disease |
|---|---|---|---|
| NCF1 | P14598 | non-pleiotropic | Granulomatous disease, chronic, cytochrome-b-positive 1, autosomal recessive (CGD1) [MIM:233700] |
| NCF2 | P19878 | non-pleiotropic | Granulomatous disease, chronic, cytochrome-b-positive 2, autosomal recessive (CGD2) [MIM:233710] |
| NCF4 | Q15080 | non-pleiotropic | Granulomatous disease, chronic, cytochrome-b-positive 3, autosomal recessive (CGD3) [MIM:613960] |
| NCSTN | Q92542 | non-pleiotropic | Acne inversa, familial, 1 (ACNINV1) [MIM:142690] |
| NDUFA1 | O15239 | non-pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] |
| NDUFAF3 | Q9BU61 | non-pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] |
| NDUFAF4 | Q9P032 | non-pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] |
| NDUFAF5 | Q5TEU4 | pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] Leigh syndrome (LS) [MIM:256000] |
| NDUFAF6 | Q330K2 | non-pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] |
| NDUFS1 | P28331 | non-pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] |
| NDUFS2 | O75306 | non-pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] |
| NDUFS7 | O75251 | non-pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] |
| NDUFS8 | O00217 | non-pleiotropic | Leigh syndrome (LS) [MIM:256000] |
| NDUFV1 | P49821 | pleiotropic | Mitochondrial complex I deficiency (MT-C1D) [MIM:252010] Leigh syndrome (LS) [MIM:256000] |
| NEK1 | Q96PY6 | non-pleiotropic | Short-rib thoracic dysplasia 6 with or without polydactyly (SRTD6) [MIM:263520] |
| NEK8 | Q86SG6 | non-pleiotropic | Nephronophthisis 9 (NPHP9) [MIM:613824] |
| NEUROG3 | Q9Y4Z2 | non-pleiotropic | Diarrhea 4, malabsorptive, congenital (DIAR4) [MIM:610370] |
| NFKBIA | P25963 | non-pleiotropic | Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency autosomal dominant (ADEDAID) [MIM:612132] |
| NFU1 | Q9UMS0 | non-pleiotropic | Multiple mitochondrial dysfunctions syndrome 1 (MMDS1) [MIM:605711] |
| NGF | P01138 | non-pleiotropic | Neuropathy, hereditary sensory and autonomic, 5 (HSAN5) [MIM:608654] |
| NHEJ1 | Q9H9Q4 | non-pleiotropic | Severe combined immunodeficiency due to NHEJ1 deficiency (NHEJ1-SCID) [MIM:611291] |
| NHLRC1 | Q6VVB1 | non-pleiotropic | Epilepsy, progressive myoclonic 2 (EPM2) [MIM:254780] |
| NHP2 | Q9NX24 | non-pleiotropic | Dyskeratosis congenita, autosomal recessive, 2 (DKCB2) [MIM:613987] |
| NIN | Q8N4C6 | non-pleiotropic | Seckel syndrome 7 (SCKL7) [MIM:614851] |
| NIPA1 | Q7RTP0 | non-pleiotropic | Spastic paraplegia 6, autosomal dominant (SPG6) [MIM:600363] |
| NIPAL4 | Q0D2K0 | non-pleiotropic | Ichthyosis, congenital, autosomal recessive 6 (ARCI6) [MIM:612281] |
| NIPBL | Q6KC79 | non-pleiotropic | Cornelia de Lange syndrome 1 (CDLS1) [MIM:122470] |
| NKX2-1 | P43699 | pleiotropic | Chorea, hereditary benign (BHC) [MIM:118700] Choreoathetosis, hypothyroidism, and neonatal respiratory distress (CHNRD) [MIM:610978] |
| NKX2-5 | P52952 | pleiotropic | Atrial septal defect 7, with or without atrioventricular conduction defects (ASD7) [MIM:108900] Hypoplastic left heart syndrome 2 (HLHS2) [MIM:614435] Hypothyroidism, congenital, non-goitrous, 5 (CHNG5) [MIM:225250] Tetralogy of Fallot (TOF) [MIM:187500] Ventricular septal defect 3 (VSD3) [MIM:614432] Asplenia, isolated congenital (ICAS) [MIM:271400] |
| NKX2-6 | A6NCS4 | non-pleiotropic | Conotruncal heart malformations (CTHM) [MIM:217095] |
| NLRP7 | Q8WX94 | non-pleiotropic | Hydatidiform mole, recurrent, 1 (HYDM1) [MIM:231090] |
| NMNAT1 | Q9HAN9 | non-pleiotropic | Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
| NNT | Q13423 | non-pleiotropic | Glucocorticoid deficiency 4 (GCCD4) [MIM:614736] |
| NOBOX | O60393 | non-pleiotropic | Premature ovarian failure 5 (POF5) [MIM:611548] |
| NODAL | Q96S42 | non-pleiotropic | Heterotaxy, visceral, 5, autosomal (HTX5) [MIM:270100] |
| NOG | Q13253 | pleiotropic | Symphalangism, proximal 1A (SYM1A) [MIM:185800] Tarsal-carpal coalition syndrome (TCC) [MIM:186570] Multiple synostoses syndrome 1 (SYNS1) [MIM:186500] Brachydactyly B2 (BDB2) [MIM:611377] |
| NOL3 | O60936 | non-pleiotropic | Myoclonus, familial cortical (FCM) [MIM:614937] |
| NOP10 | Q9NPE3 | non-pleiotropic | Dyskeratosis congenita, autosomal recessive, 1 (DKCB1) [MIM:224230] |
| NOTCH3 | Q9UM47 | pleiotropic | Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, autosomal dominant (CADASIL) [MIM:125310] Myofibromatosis, infantile 2 (IMF2) [MIM:615293] |
| NPC2 | P61916 | non-pleiotropic | Niemann-Pick disease C2 (NPC2) [MIM:607625] |
| NPHS1 | O60500 | non-pleiotropic | Nephrotic syndrome 1 (NPHS1) [MIM:256300] |
| NPHS2 | Q9NP85 | non-pleiotropic | Nephrotic syndrome 2 (NPHS2) [MIM:600995] |
| NPR2 | P20594 | non-pleiotropic | Acromesomelic dysplasia, Maroteaux type (AMDM) [MIM:602875] |
| NR0B1 | P51843 | non-pleiotropic | X-linked adrenal hypoplasia congenital (XL-AHC) [MIM:300200] |
| NR3C1 | P04150 | non-pleiotropic | Glucocorticoid resistance (GCRES) [MIM:138040] |
| NR3C2 | P08235 | pleiotropic | Early-onset hypertension with severe exacerbation in pregnancy (EOHSEP) [MIM:605115] Pseudohypoaldosteronism 1, autosomal dominant (PHA1A) [MIM:177735] |
| NRAS | P01111 | pleiotropic | Autoimmune lymphoproliferative syndrome 4 (ALPS4) [MIM:614470] Noonan syndrome 6 (NS6) [MIM:613224] |
| NSMF | Q6X4W1 | non-pleiotropic | Hypogonadotropic hypogonadism 9 with or without anosmia (HH9) [MIM:614838] |
| NSUN2 | Q08J23 | non-pleiotropic | Mental retardation, autosomal recessive 5 (MRT5) [MIM:611091] |
| NT5C3A | Q9H0P0 | non-pleiotropic | P5N deficiency (P5ND) [MIM:266120] |