Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "A"
701 to 710 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

701
Adaptor related protein complex 2 subunit mu 1
AP50, CLAPM1, MRD60, mu2
Neurodevelopmental disorder, Epilepsy with myoclonic atonic seizures, Intellectual developmental disorder seizures epilepsy, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Schizophrenia, Diabetes mellitus type 2

702
Adaptor related protein complex 2 subunit sigma 1
AP17, CLAPS2, FBH3, FBHOk, HHC3
Alzheimer disease, Autism, Calcium metabolism disorders, Neurodevelopmental disorder, Benign hypercalcemia, Hypocalciuric hypercalcemia, Non-specific syndromic intellectual disability

703
Adaptor related protein complex 3 subunit beta 1
ADTB3, ADTB3A, HPS, HPS2, PE
Asthma, Autoinflammatory syndrome, Color vision deficiency, Hermansky-pudlak syndrome, Intellectual developmental disorder, Lung disease, Major depressive disorder, Metabolic syndrome, Multiple myeloma, Neutropenia, Osteoarthritis, Pelvic organ prolapse, Pulmonary fibrosis, Thrombocytopenia, Diabetes mellitus type 2

704
Adaptor related protein complex 3 subunit beta 2
DEE48, EIEE48, NAPTB
Autism, Developmental and epileptic encephalopathy, Global developmental delay, Schizophrenia

705
Adaptor related protein complex 3 subunit delta 1
ADTD, HPS10, hBLVR
Androgenetic alopecia, Atrial fibrillation, Atrial flutter, Central nervous system cancer, Clear cell renal cell carcinoma, Early-onset severe hermansky-pudlak syndrome with hearing loss due to ap3d1 deficiency, Emphysema, Generalized epilepsy, Glioblastoma, Glioma, Hermansky-pudlak syndrome, Kidney cancer, Myocardial infarction, Ocular albinism with sensorineural deafness, Osteoarthritis
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706
Adaptor related protein complex 3 subunit mu 2
AP47B, CLA20, P47B
Cutaneous squamous cell carcinoma

707
Adaptor related protein complex 3 subunit sigma 1
CLAPS3, Sigma3A
Congenital heart disease

708
Adaptor related protein complex 3 subunit sigma 2
AP3S3, sigma3b
Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Diabetic retinopathy, Prostate cancer, Schizophrenia

709
Adaptor related protein complex 4 subunit beta 1
BETA-4, CPSQ5, SPG47
Ap-4 deficiency syndrome, Ap4-related intellectual disability and spastic paraplegia, Basal cell carcinoma, Breast cancer, Congenital neurologic anomalies, Intellectual developmental disorder, Obesity, Intellectual disability, Skin neoplasms, Spastic paraplegia, Hereditary spastic paraplegia

710
Adaptor related protein complex 4 subunit epsilon 1
CPSQ4, SPG51, STUT1
Ap-4 deficiency syndrome, Ap4-related intellectual disability and spastic paraplegia, Cerebral amyloid angiopathy, Congenital disorder of glycosylation, Congenital neurologic anomalies, Coronary artery disease, Developmental disability, Gout, Intellectual developmental disorder, Peripheral neuropathy, Intellectual disability, Spastic paraplegia, Hereditary spastic paraplegia