Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "A"
941 to 950 of 1170 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

941
ARVCF delta catenin family member
-
22q11.2 deletion syndrome, Alzheimer disease, Coronary artery disease, Digeorge syndrome, Raynaud disease, Schizophrenia, Diabetes mellitus type 2

942
Aristaless related homeobox
CT121, EIEE1, ISSX, MRX29, MRX32, MRX33, MRX36, MRX38, MRX43, MRX54, MRX76, MRX87, MRXS1, PRTS
Arachnoid cysts, Autism, Corpus callosum agenesis with abnormal genitalia, Developmental and epileptic encephalopathy, Hydranencephaly, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Lissencephaly, x-linked, X-linked intellectual disability, Partington syndrome, Periventricular heterotopia, Russell-silver syndrome, West syndrome, X-linked complex neurodevelopmental disorder, X-linked lissencephaly
View all (1 more)

943
Arsenite methyltransferase
CYT19
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Coronary artery disease, Developmental disability, Insomnia, Diabetes mellitus type 2, Lung neoplasms, Major depressive disorder, Obesity, Myocardial infarction, Neurotic disorder, Schizophrenia, Skin disease
View all (1 more)

944
N-acylsphingosine amidohydrolase 1
AC, ACDase, ASAH, PHP, PHP32, SMAPME
Arthrogryposis multiplex congenita, Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Schizophrenia, Congenital neurologic anomalies, Rolandic epilepsy, Farber disease, Lipidoses, Lipoidosis, Liver cirrhosis, Oligodendroglioma, Pena-shokeir syndrome , Spinal muscular atrophy, Diabetes mellitus type 2

945
N-acylsphingosine amidohydrolase 2
BCDase, HNAC1, LCDase, N-CDase, NCDase
Celiac disease, Estrogen-receptor negative breast cancer, Liver disease, Schizophrenia, Scoliosis

946
N-acylsphingosine amidohydrolase 2B
ASAH2C, ASAH2L, bA449O16.3, bA98I6.3
Color vision deficiency, Hyperlipidemia, Gout

947
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1
AMAP1, CENTB4, DDEF1, PAG2, PAP, ZG14P
Alzheimer disease, Juvenile arthritis, Asthma, Autism, Colorectal cancer, Melanoma, Dementia, Iga nephropathy, Juvenile idiopathic arthritis, Liver disease, Migraine, Multiple sclerosis, Obesity, Obsessive-compulsive disorder, Oligoarticular juvenile idiopathic arthritis
View all (5 more)

948
ArfGAP with SH3 domain, ankyrin repeat and PH domain 2
AMAP2, CENTB3, DDEF2, PAG3, PAP, Pap-alpha, SHAG1
Ankylosing spondylitis, Asthma, Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Coronary artery disease, Crohn disease, Glioblastoma, Glioma, Gout, Multiple sclerosis, Neuroblastoma, Oligodendroglioma, Osteoarthritis, Psoriasis
View all (2 more)

949
Ankyrin repeat and SOCS box containing 1
ASB-1
Astrocytoma, Central nervous system cancer, Obstructive pulmonary disease, Glioblastoma, Glioma, Insomnia, Multiple system atrophy

950
Ankyrin repeat and SOCS box containing 10
GLC1F
Glaucoma, Gout