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 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]