281
|
|
|
VPS26A pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
282
|
|
|
VPS26 retromer complex component B |
Pep8b |
Curated: N/A
Unreviewed: Inflammatory bowel disease, Parkinson disease
|
283
|
|
|
VPS26B pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
284
|
|
|
VPS26 endosomal protein sorting factor C |
DCRA, DSCR3, DSCRA |
Curated: Neurodevelopmental disorder, Oligodendroglioma, Diabetes mellitus type 2
Unreviewed: Colorectal Cancer, Colorectal neoplasm, Down syndrome
|
285
|
|
|
VPS26C pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
286
|
|
|
VPS28 subunit of ESCRT-I |
CIIA |
Curated: N/A
Unreviewed: Breast neoplasm, Diabetes mellitus
|
287
|
|
|
VPS29 retromer complex component |
DC15, DC7, PEP11 |
Curated: N/A
Unreviewed: Alzheimer disease, Ductal carcinoma of breast, Hepatocellular carcinoma, Parkinson disease, Schizophrenia
|
288
|
|
|
VPS33A core subunit of CORVET and HOPS complexes |
MPSPS |
Curated: Desbuquois syndrome, Mucopolysaccharidosis, mucopolysaccharidosis-plus syndrome
Unreviewed: Anemia, Arthrogryposis, Renal Dysfunction, And Cholestasis, Congenital Epicanthus, Congenital Pectus Carinatum, Congenital Pectus Excavatum, Developmental Delay, Developmental dysplasia of the hip, Edema, Glomerulosclerosis, Hermansky-Pudlak Syndrome, Hypertrophic cardiomyopathy, Kidney disease, Macroglossia, Melanoma, Mucopolysaccharidosis-Like Syndrome With Congenital Heart Defects And Hematopoietic Disorders, MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME, Obesity, Optic Atrophy, Patent ductus arteriosus, Pfaundler-Hurler Syndrome, Platelet disorder, Synophrys
|
289
|
|
|
VPS33B late endosome and lysosome associated |
KDIDAR, PFIC12 |
Curated: Arthrogryposis multiplex congenita, Arthrogryposis-renal dysfunction-cholestasis syndrome, Cholelithiasis, Kidney disease, Coronary artery disease, Hypertension, Insomnia, Metabolic syndrome, Myocardial infarction, Progressive intrahepatic cholestasis, Willis-ekbom disease, Stroke, Thrombocytopenia, Diabetes mellitus type 2
Unreviewed: Arthrogryposis, Arthrogryposis, Renal Dysfunction, And Cholestasis, Atrial Septal Defect, Blood Coagulation Disorders, Cholestasis, Cholestatic liver disease, Colorectal Cancer, Congenital anomalies of kidney and urinary tract, Congenital Ichthyosis, Conjugated hyperbilirubinemia, Conjunctivitis, Deafness, Developmental Delay, Diabetes Mellitus, Essential tremor, Fanconi syndrome, Hemorrhage, Hypothyroidism, Ichthyosis, Intrahepatic Cholestasis, Kidney Disease, Liver Cancer, Liver carcinoma, Microcephaly, Micrognathism, Multiple Congenital Anomalies, Multiple system atrophy, Myocardial Infarction, Nasopharyngeal Carcinoma, Neoplasms, Nephrocalcinosis, Platelet disorder, Proteinuria, Pruritus, Vacuolar Myopathy, Ventricular hypertrophy, Ventricular septal defect
|
290
|
|
|
VPS33B divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|