|
1031
|
|
|
Cat eye syndrome chromosome region |
CES |
|
|
1032
|
|
|
ARF like GTPase 6 interacting protein 5 |
DERP11, GTRAP3-18, HSPC127, JWA, PRAF3, Yip6b, addicsin, hp22, jmx |
|
|
1033
|
|
|
Anterior gradient 2, protein disulphide isomerase family member |
AG-2, AG2, GOB-4, HAG-2, HEL-S-116, HPC8, PDIA17, RIFTD, XAG-2 |
|
|
1034
|
|
|
Actin related protein 2/3 complex subunit 1A |
Arc40, HEL-68, HEL-S-307, SOP2Hs, SOP2L |
|
|
1035
|
|
|
HIV-1 Tat interactive protein 2 |
CC3, SDR44U1, TIP30 |
|
|
1036
|
|
|
1-acylglycerol-3-phosphate O-acyltransferase 1 |
1-AGPAT1, G15, LPAAT-alpha, LPAATA, LPLAT1 |
|
|
1037
|
|
|
1-acylglycerol-3-phosphate O-acyltransferase 2 |
1-AGPAT2, BSCL, BSCL1, LPAAB, LPAAT-beta, LPLAT2 |
Acanthosis nigricans, Atherosclerosis, Atrial fibrillation, Cirrhosis, Congenital exomphalos, Congenital lipodystrophy, Congestive heart failure, Diabetes mellitus, Fatty liver, Hyperinsulinism, Hypertrophic cardiomyopathy, Hypertrophy of clitoris, Immunologic deficiency syndromes, Isolated somatotropin deficiency, Kidney disease, Lipoatrophy, Lipodystrophy, Liver failure, Macrotia, Malocclusion, Mental retardation, Myocardial infarction, Myopathy, Nephrolithiasis, Nervous system diseases, Osteopenia, Osteoporosis, Pancreatitis, Polycystic ovary syndrome, Precocious puberty, Pulmonary arterial hypertension, Renal glomerular disease, Renal insufficiency, Scoliosis, Secondary physiologic amenorrhea, Somatotropin deficiency, Talipes transversoplanus, Ventricular hypertrophyView all (23 more) |
|
1038
|
|
|
Ribonuclease P/MRP subunit p38 |
- |
|
|
1039
|
|
|
Serine palmitoyltransferase long chain base subunit 1 |
ALS27, HSAN1, HSN1, LBC1, LCB1, SPT1, SPTI |
Bipolar disorder, Breast cancer, Charcot-marie-tooth disease, Dysautonomia, Foot osteomyelitis, Hearing loss, Hereditary sensory and autonomic neuropathy, Mental disorders, Neuropathy, Psychosis, Schizophrenia, Sensorimotor neuropathy, Sensory and autonomic neuropathy |
|
1040
|
|
|
Solute carrier family 35 member A1 |
CDG2F, CMPST, CST, hCST |
Aortic valve insufficiency, Clinodactyly, Congenital disorder of glycosylation, Developmental delay, Dysarthria, Epileptic encephalopathy, Orofacial dyskinesia, Macrothrombocytopenia, Mental retardation, Microcephaly, Neck webbing, Neutropenia, Nystagmus, Subcutaneous hemorrhage |
