|
761
|
|
|
Adrenomedullin 2 |
AM2, dJ579N16.4 |
|
|
762
|
|
|
Alpha tubulin acetyltransferase 1 |
C6orf134, MEC17, Nbla00487, TAT, alpha-TAT, alpha-TAT1 |
|
|
763
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 20 |
ADAM-TS20, ADAMTS-20, GON-1 |
|
|
764
|
|
|
Asparaginase and isoaspartyl peptidase 1 |
ALP, ALP1, CRASH |
|
|
765
|
|
|
Armadillo repeat containing 9 |
ARM, JBTS30, KU-MEL-1, NS21 |
Cerebellar vermis agenesis, Congenital cerebral hernia, Congenital coloboma of iris, Developmental delay, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Mental retardation, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Polydactyly of toes, Polymicrogyria, Ptosis, Scoliosis, Situs inversus, StrabismusView all (3 more) |
|
766
|
|
|
Alpha kinase 1 |
8430410J10Rik, LAK, ROSAH |
Anhidrosis, Atrial fibrillation, Diabetes mellitus, Diabetic nephropathy, Glomerulosclerosis, Gout, Nephrosclerosis, Obesity, Optic nerve oedema, Ovarian adenocarcinoma, Retinal dystrophy, Rheumatoid arthritis |
|
767
|
|
|
ADAM metallopeptidase domain 33 |
C20orf153, DJ964F7.1 |
|
|
768
|
|
|
ADAM metallopeptidase domain 12 |
ADAM12-OT1, CAR10, MCMP, MCMPMltna, MLTN, MLTNA |
|
|
769
|
|
|
Acyl-CoA dehydrogenase family member 10 |
- |
|
|
770
|
|
|
ASXL transcriptional regulator 3 |
BRPS, KIAA1713 |
Angelman syndrome, Anxiety disorder, Arachnodactyly, Asthma, Autism, Bainbridge-ropers syndrome, Developmental delay, Dolichocephaly, Dysmorphic features, Dyssomnia, Epilepsy, Esotropia, Glossoptosis, Hand flapping, Hearing loss, High palate, Hypoplasia of corpus callosum, Mental retardation, Laryngomalacia, Macrostomia, Madelung deformity, Mental depression, Metopic synostosis, Microcephaly, Multiple congenital anomalies, Neurodevelopmental disorders, Posteriorly rotated ear, Scoliosis, Sleep disorders, Strabismus, Synophrys, T-cell lymphomaView all (17 more) |
