Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 13 of 33)
| Gene | UniProt | Protein Type | Disease |
|---|---|---|---|
| GM2A | P17900 | non-pleiotropic | GM2-gangliosidosis AB (GM2GAB) [MIM:272750] |
| GMPPA | Q96IJ6 | non-pleiotropic | Alacrima, achalasia, and mental retardation syndrome (AAMR) [MIM:615510] |
| GNA11 | P29992 | pleiotropic | Hypocalcemia, autosomal dominant 2 (HYPOC2) [MIM:615361] Hypocalciuric hypercalcemia, familial 2 (HHC2) [MIM:145981] |
| GNAI3 | P08754 | non-pleiotropic | Auriculocondylar syndrome 1 (ARCND1) [MIM:602483] |
| GNAL | P38405 | non-pleiotropic | Dystonia 25 (DYT25) [MIM:615073] |
| GNAO1 | P09471 | non-pleiotropic | Epileptic encephalopathy, early infantile, 17 (EIEE17) [MIM:615473] |
| GNAS | P63092 | pleiotropic | Albright hereditary osteodystrophy (AHO) [MIM:103580] ACTH-independent macronodular adrenal hyperplasia (AIMAH) [MIM:219080] McCune-Albright syndrome (MAS) [MIM:174800] Pseudohypoparathyroidism 1A (PHP1A) [MIM:103580] Progressive osseous heteroplasia (POH) [MIM:166350] Pseudohypoparathyroidism 1C (PHP1C) [MIM:612462] |
| GNAT1 | P11488 | non-pleiotropic | Night blindness, congenital stationary, autosomal dominant 3 (CSNBAD3) [MIM:610444] |
| GNB4 | Q9HAV0 | non-pleiotropic | Charcot-Marie-Tooth disease, dominant, intermediate type, F (CMTDIF) [MIM:615185] |
| GNE | Q9Y223 | pleiotropic | Inclusion body myopathy 2 (IBM2) [MIM:600737] Sialuria (SIALURIA) [MIM:269921] Nonaka myopathy (NM) [MIM:605820] |
| GNMT | Q14749 | non-pleiotropic | Glycine N-methyltransferase deficiency (GNMT deficiency) [MIM:606664] |
| GNPAT | O15228 | non-pleiotropic | Rhizomelic chondrodysplasia punctata 2 (RCDP2) [MIM:222765] |
| GNPTG | Q9UJJ9 | non-pleiotropic | Mucolipidosis type III complementation group C (MLIIIC) [MIM:252605] |
| GNS | P15586 | non-pleiotropic | Mucopolysaccharidosis 3D (MPS3D) [MIM:252940] |
| GOSR2 | O14653 | non-pleiotropic | Epilepsy, progressive myoclonic 6 (EPM6) [MIM:614018] |
| GP6 | Q9HCN6 | non-pleiotropic | Bleeding disorder, platelet-type 11 (BDPLT11) [MIM:614201] |
| GP9 | P14770 | non-pleiotropic | Bernard-Soulier syndrome (BSS) [MIM:231200] |
| GPHN | Q9NQX3 | non-pleiotropic | Molybdenum cofactor deficiency, complementation group C (MOCODC) [MIM:615501] |
| GPI | P06744 | non-pleiotropic | Hemolytic anemia, non-spherocytic, due to glucose phosphate isomerase deficiency (HA-GPID) [MIM:613470] |
| GPR179 | Q6PRD1 | non-pleiotropic | Night blindness, congenital stationary, 1E (CSNB1E) [MIM:614565] |
| GPR56 | Q9Y653 | non-pleiotropic | Polymicrogyria, bilateral frontoparietal (BFPP) [MIM:606854] |
| GRIA3 | P42263 | non-pleiotropic | Mental retardation, X-linked 94 (MRX94) [MIM:300699] |
| GRIN1 | Q05586 | non-pleiotropic | Mental retardation, autosomal dominant 8 (MRD8) [MIM:614254] |
| GRIN2A | Q12879 | non-pleiotropic | Epilepsy, focal, with speech disorder and with or without mental retardation (FESD) [MIM:245570] |
| GRIN2B | Q13224 | non-pleiotropic | Mental retardation, autosomal dominant 6 (MRD6) [MIM:613970] |
| GRK1 | Q15835 | non-pleiotropic | Night blindness, congenital stationary, Oguchi type 2 (CSNBO2) [MIM:613411] |
| GRM6 | O15303 | non-pleiotropic | Night blindness, congenital stationary, 1B (CSNB1B) [MIM:257270] |
| GRXCR1 | A8MXD5 | non-pleiotropic | Deafness, autosomal recessive, 25 (DFNB25) [MIM:613285] |
| GSN | P06396 | non-pleiotropic | Amyloidosis 5 (AMYL5) [MIM:105120] |
| GTF2H5 | Q6ZYL4 | non-pleiotropic | Trichothiodystrophy photosensitive (TTDP) [MIM:601675] |
| GUCA1B | Q9UMX6 | non-pleiotropic | Retinitis pigmentosa 48 (RP48) [MIM:613827] |
| GUCY2C | P25092 | pleiotropic | Diarrhea 6 (DIAR6) [MIM:614616] Meconium ileus (MECIL) [MIM:614665] |
| GUSB | P08236 | non-pleiotropic | Mucopolysaccharidosis 7 (MPS7) [MIM:253220] |
| GYG1 | P46976 | non-pleiotropic | Glycogen storage disease 15 (GSD15) [MIM:613507] |
| GYS2 | P54840 | non-pleiotropic | Glycogen storage disease 0 (GSD0) [MIM:240600] |
| H6PD | O95479 | non-pleiotropic | Cortisone reductase deficiency (CRD) [MIM:604931] |
| HADHB | P55084 | non-pleiotropic | Trifunctional protein deficiency (TFP deficiency) [MIM:609015] |
| HAL | P42357 | non-pleiotropic | Histidinemia (HISTID) [MIM:235800] |
| HAMP | P81172 | non-pleiotropic | Hemochromatosis 2B (HFE2B) [MIM:613313] |
| HARS | P12081 | non-pleiotropic | Usher syndrome 3B (USH3B) [MIM:614504] |
| HARS2 | P49590 | non-pleiotropic | Perrault syndrome 2 (PRLTS2) [MIM:614926] |
| HAX1 | O00165 | non-pleiotropic | Neutropenia, severe congenital 3, autosomal recessive (SCN3) [MIM:610738] |
| HCCS | P53701 | non-pleiotropic | Microphthalmia, syndromic, 7 (MCOPS7) [MIM:309801] |
| HCFC1 | P51610 | non-pleiotropic | Mental retardation, X-linked 3 (MRX3) [MIM:309541] |
| HCRT | O43612 | non-pleiotropic | Narcolepsy 1 (NRCLP1) [MIM:161400] |
| HEATR2 | Q86Y56 | non-pleiotropic | Ciliary dyskinesia, primary, 18 (CILD18) [MIM:614874] |
| HES7 | Q9BYE0 | non-pleiotropic | Spondylocostal dysostosis 4, autosomal recessive (SCDO4) [MIM:613686] |
| HEXB | P07686 | non-pleiotropic | GM2-gangliosidosis 2 (GM2G2) [MIM:268800] |
| HFE2 | Q6ZVN8 | non-pleiotropic | Hemochromatosis 2A (HFE2A) [MIM:602390] |
| HGD | Q93099 | non-pleiotropic | Alkaptonuria (AKU) [MIM:203500] |