411
|
|
|
AHNAK nucleoprotein 2 |
C14orf78 |
|
412
|
|
|
Aryl hydrocarbon receptor |
FVH3, RP85, bHLHe76 |
Ankylosing spondylitis, Experimental arthritis, Rheumatoid arthritis, Atherosclerosis, Atrophy, Autism, Basal cell carcinoma, Behcet disease, Bladder calculus, Bone disease, Bone resorption, Breast cancer, Breast neoplasms, Cancer, Cardiomegaly, Chronobiology disorder, Colitis, Color vision deficiency, Colorectal cancer, Congenital heart defects, Congenital heart disease, Congenital nystagmus, Conotruncal cardiac defect, Contact dermatitis, Craniofacial abnormalities, Crohn disease, Melanoma, Cutaneous squamous cell carcinoma, Atopic dermatitis, Dyslexia, Edema, Estrogen-receptor negative breast cancer, Growth disorder, Congenital heart defect, Hepatomegaly, Hyperoxia, Hypertension, Hypertrophy, Hypoglycemia, Female infertility, Male infertility, Diabetes mellitus type 2, Keratosis, Left ventricular disease, Liver cirrhosis, Liver disease, Liver neoplasms, Lung cancer, Metabolic syndrome, Necrosis, Nonalcoholic fatty liver disease, Nystagmus, Obesity, Ovarian cancer, Ovarian serous carcinoma, Pancreatic cancer, Pancreatic neoplasms, Patent ductus venosus, Prostate cancer, Prostatic neoplasms, Pruritus, Psoriasis, Pulmonary arterial hypertension, Respiratory system disease, Retinitis pigmentosa, Sclerosing cholangitis, Skin cancer, Skin disease, Skin neoplasms, Splenic disease, Splenomegaly, Squamous cell carcinoma, Stomach neoplasms, Diabetes mellitus type 1, Ulcerative colitis, Ureteral neoplasms, Urinary bladder calculi, Urinary bladder stone, Urolithiasis, Vascular diseaseView all (65 more) |
413
|
|
|
Aryl hydrocarbon receptor repressor |
AHH, AHHR, bHLHe77 |
|
414
|
|
|
Alpha 2-HS glycoprotein |
A2HS, AHS, APMR1, FETUA, HSGA |
Alopecia-intellectual disability syndrome, Amr syndrome, Calcinosis, Ischemic heart disease, Coronary artery disease, Diabetes mellitus type 2, Kidney failure, Myocardial ischemia, Nephrolithiasis, Otosclerosis, Perniola krajewska carnevale syndrome |
415
|
|
|
Activation induced cytidine deaminase |
AID, ARP2, CDA2, HEL-S-284, HIGM2 |
|
416
|
|
|
Axin interactor, dorsalization associated |
C1orf80 |
|
417
|
|
|
Allograft inflammatory factor 1 |
AIF-1, IBA1, IRT-1, IRT1 |
Breast cancer, Cancer, Colorectal cancer, Coronary artery disease, Diabetes mellitus type 1, Hypertension, Estrogen-receptor negative breast cancer, Gallstones, Hyperalgesia, Inflammatory bowel disease, Lewy body disease, Liver cirrhosis, Lung cancer, Major depressive disorder, Myocardial infarction, Non-hodgkins lymphoma, Ovarian cancer, Ovarian serous carcinoma, Parkinson disease, Prostate cancer, Psoriasis, Rheumatoid arthritis, Squamous cell carcinoma, Stevens-johnson syndrome, Systemic lupus erythematosus, Toxic epidermal necrolysis, Trigeminal neuralgiaView all (12 more) |
418
|
|
|
Apoptosis inducing factor mitochondria associated 1 |
AIF, AUNX1, CMT2D, CMTX4, COWCK, COXPD6, DFNX5, NADMR, NAMSD, PDCD8, SEMDHL |
Auditory neuropathy, Autism, Beta-hydroxyisobutyryl-coa deacylase deficiency, Bipolar disorder, Charcot-marie-tooth disease, Charcot-marie-tooth disease, x-linked, Combined oxidative phosphorylation deficiency, Congenital ear anomaly, Cowchock syndrome, Deafness, x-linked, Dejerine-sottas disease, Desbuquois syndrome, Experimental diabetes, Diabetes mellitus type 1, Hereditary motor and sensory neuropathies, Huntington disease, Hypertrophic neuropathy, Leigh syndrome, Leukodystrophy, Necrosis, Peripheral neuropathy, Peroneal muscle atrophy, Retinal detachment, Roussy-levy syndrome, Hearing loss, Spondyloepimetaphyseal dysplasia, X-linked hereditary sensory and autonomic neuropathy with deafness, X-linked hereditary sensory and autonomic neuropathy with hearing lossView all (13 more) |
419
|
|
|
AIF family member 2 |
AMID, FSP1, PRG3 |
|
420
|
|
|
AIF family member 3 |
AIFL |
|
