31
|
|
|
Aminoadipate aminotransferase |
KAT2, KATII, KYAT2 |
Curated: Hepatocellular carcinoma, Dementia, Major depressive disorder, Multiple myeloma
Unreviewed: Anxiety disorder, Autism, Autism Spectrum Disorder, Crohn Disease, Detrusor And Sphincter Dyssynergia, Huntington Disease, Leiomyoma, Liver carcinoma, Mental Depression, Mental Disorders, Mitochondrial disease, Neoplasms, Neurodegenerative disorder, Schizophrenia, Sex Differentiation Disorders, Stomach neoplasms, Ulcerative colitis
|
32
|
|
|
Alpha and gamma adaptin binding protein |
KPPP1, PPKP1, PPKP1A, p34 |
Curated: Cardiovascular disease, Gastroesophageal reflux disease, Keratosis palmoplantaris papulosa
Unreviewed: Ataxia Telangiectasia, Bladder carcinoma, Breast Carcinoma, Breast neoplasm, Cardiovascular Diseases, Colonic Neoplasms, Congenital heart defects, Dermatologic Disorders, Developmental dysplasia of the hip, Hodgkin Disease, Keratosis Palmoplantaris Papulosa, Lung Cancer, Lung carcinoma, Meleda Disease, Multiple polyposis syndrome, Neoplasms, Palmoplantar keratoderma, Pancreatic Neoplasm, Punctate Keratosis, Punctate palmoplantar hyperkeratosis, Punctate Palmoplantar Keratoderma, Renal Carcinoma, Skin disease, Xeroderma Pigmentosum
|
33
|
|
|
AP2 associated kinase 1 |
- |
Curated: Coronary artery disease, Dental caries, Gout, Parkinson disease, Periodontal disease, Periodontitis, Tooth agenesis
Unreviewed: Amyotrophic Lateral Sclerosis, Diabetes, Diabetes Mellitus, Septicemia, Urinary bladder neoplasms
|
34
|
|
|
Adipogenesis associated Mth938 domain containing |
C11orf67, CK067, PTD015 |
Curated: Central nervous system cancer, Glioblastoma, Glioma, Graves disease, Prostate cancer, Thyrotoxic periodic paralysis
Unreviewed: Graves Disease, Thyrotoxic Periodic Paralysis
|
35
|
|
|
Angio associated migratory cell protein |
- |
Curated: Smooth surface dental caries
Unreviewed: Breast Cancer, Breast Carcinoma, Ductal carcinoma, Intervertebral disc disease, Lung Cancer, Lung carcinoma, Malignant Neoplasm
|
36
|
|
|
Aralkylamine N-acetyltransferase |
DSPS, SNAT |
Curated: Bipolar depression, Major depressive disorder, Sleep disorder
Unreviewed: Adrenal Cortical Hypofunction, Advanced Sleep Phase Syndrome, Androgen-Insensitivity Syndrome, Asthma, Autism, Autism Spectrum Disorder, Bipolar Disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cholestasis, Colorectal Cancer, Colorectal neoplasm, Delayed Sleep Phase Syndrome, Hematologic disease, Immune system disease, Liver Fibrosis, Malignant Neoplasm, Melanoma, Mental Depression, Neoplasms, Non-24 Hour Sleep-Wake Disorder, Nonorganic Sleep Wake Cycle Disorders, Prostatic neoplasm, Retinoblastoma, Shift-Work Sleep Disorder, Systemic lupus erythematosus, Ulcerative colitis
|
37
|
|
|
AAR2 splicing factor |
C20orf4, CGI-23 |
Curated: Cerebellar malformation, Global developmental delay, Non-melanoma skin carcinoma, Obesity, Ventricular septal defect
Unreviewed: Developmental Delay, Hypoplasia Of Corpus Callosum, Melanoma, Patent foramen ovale
|
38
|
|
|
Alanine and arginine rich domain containing protein |
C8orf85 |
Curated: Eczema, Hypertension, Major depressive disorder, Thoracic aortic aneurysm
Unreviewed: N/A
|
39
|
|
|
Alanyl-tRNA synthetase 1 |
AARS, CMT2N, DEE29, EIEE29, HDLS2, TTD8 |
Curated: Leukoencephalopathy, Charcot-marie-tooth disease, Congenital clubfoot, Dejerine-sottas disease, Developmental and epileptic encephalopathy, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Leukodystrophy, Osteoarthritis, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Trichothiodystrophy, Charcot-Marie-Tooth disease axonal type 2N, developmental and epileptic encephalopathy, 29
Unreviewed: Antithrombin deficiency, Attention Deficit Hyperactivity Disorder, Autism, Blepharospasm, Brain disease, Breast Cancer, Breast Carcinoma, Carcinogenesis, Cardiomyopathy, Cerebral Atrophy, Charcot-Marie-Tooth Disease, Demyelinating diseases, Dermatomyositis, Developmental Delay, Developmental regression, Distal hereditary motor neuropathy, Dwarfism, Dysautonomia, Dyskinetic Syndrome, Ectrodactyly, Epilepsy, Epileptic encephalopathy, Gastroesophageal Reflux Disease, Hearing Loss, Hereditary Diffuse Leukoencephalopathy With Spheroids, Hypodontia, Inflammatory Myopathy, Lung disease, Mental retardation, Metachromatic leukodystrophy, Microcephaly, Mitochondrial disease, Motor nerve neuritis, Multiple myeloma, Myositis, Myotonic dystrophy, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neuropathy, Non-Specifi Epileptic Encephalopathy, Nystagmus, Optic Atrophy, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polymyositis, Ptosis, Status Epilepticus, Upper extremity deformity, congenital, West Syndrome
|
40
|
|
|
Alanyl-tRNA synthetase 1 pseudogene 1 |
AARSP1 |
Curated: N/A
Unreviewed: N/A
|