|
741
|
|
|
Phospholipid scramblase 4 |
TRA1 |
|
|
742
|
|
|
Proteasome 26S subunit, non-ATPase 3 |
P58, RPN3, S3, TSTA2 |
|
|
743
|
|
|
Patatin like domain 2, triacylglycerol lipase |
1110001C14Rik, ATGL, FP17548, PEDF-R, TTS-2.2, TTS2, iPLA2zeta |
Cardiomyopathy, Cholecystitis, Congestive heart failure, Diabetes mellitus, Dwarfism, Dysmorphic features, Fatty liver, Hearing loss, Heart diseases, Limb muscle atrophy, Mental retardation, Motor delay, Myopathy, Neutral lipid storage myopathy, Sclerocystic ovaries, Pancreatitis, Polycystic ovary syndrome, Triglyceride deposit cardiomyovasculopathyView all (3 more) |
|
744
|
|
|
Decaprenyl diphosphate synthase subunit 2 |
C6orf210, COQ10D3, COQ1B, DLP1, bA59I9.3, hDLP1 |
Bilateral convulsive seizures, Central visual impairment, Chronic obstructive pulmonary disease, Coenzyme q10 deficiency, Developmental regression, Diabetes mellitus, Hypoalbuminemia, Leigh syndrome, Leigh syndrome with nephrotic syndrome, Hypotonia, Nephritis, Nephrotic syndrome, Renal cyst, Status epilepticus |
|
745
|
|
|
Proteasome 26S subunit, non-ATPase 5 |
S5B |
|
|
746
|
|
|
Plexin domain containing 1 |
TEM3, TEM7 |
|
|
747
|
|
|
P21 (RAC1) activated kinase 5 |
PAK7 |
|
|
748
|
|
|
Pellino E3 ubiquitin protein ligase 1 |
- |
|
|
749
|
|
|
Proteasome 26S subunit, non-ATPase 12 |
Rpn5, STISS, p55 |
17q24.2 microdeletion syndrome, Cubitus valgus, Anxiety disorder, Dermatitis, Developmental delay, Hallucinations, Mental retardation, Micrognathism, Microtia, Mood swings, Motor delay, Myopia, Otitis media, Otosclerosis, Patent ductus arteriosus, Ptosis, Pulmonary stenosis, Scoliosis, Secondary physiologic amenorrhea, Stankiewicz-isidor syndrome, Syndromic mental retardation, Synophrys, Vesicoureteral refluxView all (8 more) |
|
750
|
|
|
Proteasome activator subunit 1 |
HEL-S-129m, IFI5111, PA28A, PA28alpha, REGalpha |
|
