Found 257 pleiotropic proteins (16.0 %) and 1345 non-pleiotropic proteins (84.0 %).
1602 items found (page 18 of 33)
Gene | UniProt | Protein Type | Disease |
---|---|---|---|
MASP2 | O00187 | non-pleiotropic | MASP2 deficiency (MASPD) [MIM:613791] |
MASTL | Q96GX5 | non-pleiotropic | Thrombocytopenia 2 (THC2) [MIM:188000] |
MATR3 | P43243 | non-pleiotropic | Amyotrophic lateral sclerosis 21 (ALS21) [MIM:606070] |
MBTPS2 | O43462 | pleiotropic | IFAP syndrome with or without BRESHECK syndrome (IFAPS) [MIM:308205] Keratosis follicularis spinulosa decalvans X-linked (KFSDX) [MIM:308800] |
MC2R | Q01718 | non-pleiotropic | Glucocorticoid deficiency 1 (GCCD1) [MIM:202200] |
MC4R | P32245 | non-pleiotropic | Obesity (OBESITY) [MIM:601665] |
MCCC1 | Q96RQ3 | non-pleiotropic | Methylcrotonoyl-CoA carboxylase 1 deficiency (MCC1D) [MIM:210200] |
MCCC2 | Q9HCC0 | non-pleiotropic | Methylcrotonoyl-CoA carboxylase 2 deficiency (MCC2D) [MIM:210210] |
MCFD2 | Q8NI22 | non-pleiotropic | Factor V and factor VIII combined deficiency 2 (F5F8D2) [MIM:613625] |
MCOLN1 | Q9GZU1 | non-pleiotropic | Mucolipidosis type IV (MLIV) [MIM:252650] |
MCPH1 | Q8NEM0 | non-pleiotropic | Microcephaly 1, primary, autosomal recessive (MCPH1) [MIM:251200] |
MECP2 | P51608 | pleiotropic | Rett syndrome (RTT) [MIM:312750] Mental retardation, X-linked, syndromic, 13 (MRXS13) [MIM:300055] |
MED13L | Q71F56 | non-pleiotropic | Transposition of the great arteries dextro-looped 1 (DTGA1) [MIM:608808] |
MED17 | Q9NVC6 | non-pleiotropic | Microcephaly, postnatal progressive, with seizures and brain atrophy (MCPHSBA) [MIM:613668] |
MED23 | Q9ULK4 | non-pleiotropic | Mental retardation, autosomal recessive 18 (MRT18) [MIM:614249] |
MED25 | Q71SY5 | non-pleiotropic | Charcot-Marie-Tooth disease 2B2 (CMT2B2) [MIM:605589] |
MEGF8 | Q7Z7M0 | non-pleiotropic | Carpenter syndrome 2 (CRPT2) [MIM:614976] |
MEN1 | O00255 | pleiotropic | Familial multiple endocrine neoplasia type I (MEN1) [MIM:131100] Familial isolated hyperparathyroidism (FIHP) [MIM:145000] |
MERTK | Q12866 | non-pleiotropic | Retinitis pigmentosa 38 (RP38) [MIM:613862] |
MET | P08581 | pleiotropic | Renal cell carcinoma papillary (RCCP) [MIM:605074] Hepatocellular carcinoma (HCC) [MIM:114550] |
MFSD8 | Q8NHS3 | non-pleiotropic | Ceroid lipofuscinosis, neuronal, 7 (CLN7) [MIM:610951] |
MGAT2 | Q10469 | non-pleiotropic | Congenital disorder of glycosylation 2A (CDG2A) [MIM:212066] |
MGME1 | Q9BQP7 | non-pleiotropic | Mitochondrial DNA depletion syndrome 11 (MTDPS11) [MIM:615084] |
MIB1 | Q86YT6 | non-pleiotropic | Left ventricular non-compaction 7 (LVNC7) [MIM:615092] |
MID1 | O15344 | non-pleiotropic | Opitz GBBB syndrome 1 (OGS1) [MIM:300000] |
MIP | P30301 | non-pleiotropic | Cataract 15, multiple types (CTRCT15) [MIM:615274] |
MKRN3 | Q13064 | non-pleiotropic | Precocious puberty, central 2 (CPPB2) [MIM:615346] |
MLC1 | Q15049 | non-pleiotropic | Leukoencephalopathy, megalencephalic, with subcortical cysts, 1 (MLC1) [MIM:604004] |
MLPH | Q9BV36 | non-pleiotropic | Griscelli syndrome 3 (GS3) [MIM:609227] |
MMAA | Q8IVH4 | non-pleiotropic | Methylmalonic aciduria type cblA (MMAA) [MIM:251100] |
MMAB | Q96EY8 | non-pleiotropic | Methylmalonic aciduria type cblB (MMAB) [MIM:251110] |
MMACHC | Q9Y4U1 | non-pleiotropic | Methylmalonic aciduria and homocystinuria type cblC (MMAHCC) [MIM:277400] |
MMADHC | Q9H3L0 | non-pleiotropic | Methylmalonic aciduria and homocystinuria type cblD (MMAHCD) [MIM:277410] |
MMP14 | P50281 | non-pleiotropic | Winchester syndrome (WNCHRS) [MIM:277950] |
MMP2 | P08253 | non-pleiotropic | Multicentric osteolysis, nodulosis, and arthropathy (MONA) [MIM:259600] |
MNX1 | P50219 | non-pleiotropic | Currarino syndrome (CURRAS) [MIM:176450] |
MOCOS | Q96EN8 | non-pleiotropic | Xanthinuria 2 (XU2) [MIM:603592] |
MOCS1 | Q9NZB8 | non-pleiotropic | Molybdenum cofactor deficiency, complementation group A (MOCODA) [MIM:252150] |
MOCS2 | O96007 | non-pleiotropic | Molybdenum cofactor deficiency, complementation group B (MOCODB) [MIM:252160] |
MOCS2 | O96033 | non-pleiotropic | Molybdenum cofactor deficiency, complementation group B (MOCODB) [MIM:252160] |
MOG | Q16653 | non-pleiotropic | Narcolepsy 7 (NRCLP7) [MIM:614250] |
MOGS | Q13724 | non-pleiotropic | Type IIb congenital disorder of glycosylation (CDGIIb) [MIM:606056] |
MPC1 | Q9Y5U8 | non-pleiotropic | Mitochondrial pyruvate carrier deficiency (MPYCD) [MIM:614741] |
MPDU1 | O75352 | non-pleiotropic | Congenital disorder of glycosylation 1F (CDG1F) [MIM:609180] |
MPI | P34949 | non-pleiotropic | Congenital disorder of glycosylation 1B (CDG1B) [MIM:602579] |
MPLKIP | Q8TAP9 | non-pleiotropic | Trichothiodystrophy non-photosensitive 1 (TTDN1) [MIM:234050] |
MPV17 | P39210 | non-pleiotropic | Mitochondrial DNA depletion syndrome 6 (MTDPS6) [MIM:256810] |
MRE11A | P49959 | non-pleiotropic | Ataxia-telangiectasia-like disorder (ATLD) [MIM:604391] |
MRPL3 | P09001 | non-pleiotropic | Combined oxidative phosphorylation deficiency 9 (COXPD9) [MIM:614582] |
MRPL44 | Q9H9J2 | non-pleiotropic | Combined oxidative phosphorylation deficiency 16 (COXPD16) [MIM:615395] |