Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
701 to 710 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

701
163
Adaptor related protein complex 2 subunit beta 1
ADTB2, AP105B, AP2-BETA, CLAPB1
Idiopathic pulmonary fibrosis, Schizophrenia, Depression, Uveal melanoma

702
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

703
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

704
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

705
Adaptor related protein complex 3 subunit beta 2
DEE48, EIEE48, NAPTB
Autism, Developmental and epileptic encephalopathy, Global developmental delay, Schizophrenia

706
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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707
Adaptor related protein complex 3 subunit mu 2
AP47B, CLA20, P47B
Cutaneous squamous cell carcinoma

708
Adaptor related protein complex 3 subunit sigma 1
CLAPS3, Sigma3A
Congenital heart disease, Liver cirrhosis

709
Adaptor related protein complex 3 subunit sigma 2
AP3S3, sigma3b
Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Diabetic retinopathy, Prostate cancer, Schizophrenia, Diabetes mellitus, type 2

710
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 neoplasm, Spastic paraplegia, Hereditary spastic paraplegia