241
|
|
|
Acyl-CoA synthetase family member 3 |
- |
|
242
|
|
|
Allograft inflammatory factor 1 |
AIF-1, IBA1, IRT-1, IRT1 |
|
243
|
|
|
ALG14 UDP-N-acetylglucosaminyltransferase subunit |
CMS15, IDDEBF, MEPCA |
|
244
|
|
|
Alpha-2-macroglobulin |
A2MD, CPAMD5, FWP007, S863-7 |
Alpha-2-macroglobulin deficiency, Alzheimer disease, Colonic neoplasms, Dementia, Hepatocellular adenoma, Hepatolenticular degeneration, Kidney failure, Liver carcinoma, Liver cirrhosis, Liver fibrosis, Lung neoplasms, Lung cancer, Lung diseases, Mental depression, Nephrotic syndrome, Parkinson disease, Acute kidney insufficiency, Senile dementiaView all (3 more) |
245
|
|
|
Apolipoprotein B mRNA editing enzyme catalytic subunit 3A |
A3A, ARP3, PHRBN, bK150C2.1 |
Arthritis, Benign neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Juvenile arthritis, Malignant neoplasm, Marfan syndrome, Neoplasms, Nonorganic psychosis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Psychosis, Still disease |
246
|
|
|
ALMS1 pseudogene 1 |
ALMS1L, ALMS1P |
|
247
|
|
|
Ankyrin repeat domain 23 |
DARP, MARP3 |
|
248
|
|
|
Aprataxin and PNKP like factor |
APFL, C2orf13, PALF, Xip1, ZCCHH1 |
|
249
|
|
|
ARF like GTPase 13B |
ARL2L1, JBTS8 |
Bilateral hypermetropia, Cerebellar vermis agenesis, Ciliopathies, Congenital cerebral hernia, Congenital coloboma of iris, Developmental delay, Diastrophic dysplasia, Disorder of eye, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Keratosis follicularis, Mental retardation, Nystagmus, Obesity, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Polydactyly of toes, Polymicrogyria, Ptosis, Retinal dystrophy, Retinitis pigmentosa, Scoliosis, Situs inversus, StrabismusView all (11 more) |
250
|
|
|
Rho GTPase activating protein 27 |
CAMGAP1, PP905, SH3D20, SH3P20 |
|