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"
1151 to 1160 of 1165 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1151
Advillin
ADVIL, DOC6, NPHS21, p92
Combined oxidative phosphorylation deficiency, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Steroid-resistant nephrotic syndrome

1152
AVL9 cell migration associated
KIAA0241
Alzheimer disease, Juvenile arthritis, Insomnia, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

1153
Arginine vasopressin
ADH, ARVP, AVP-NPII, AVRP, VP
Amnesia, Angina pectoris, Cardiac arrhythmias, Autism, Bipolar disorder, Cardiac arrhythmia, Cardiomyopathy, Neurogenic diabetes insipidus, Congestive heart failure, Depression, Diabetes insipidus, Arginine vasopressin deficiency, Gastrointestinal hemorrhage, Heart failure, Hereditary arginine vasopressin deficiency
View all (13 more)

1154
Arginine vasopressin induced 1
PP5395, VIP32, VIT32
Alzheimer disease, Lung neoplasms

1155
Arginine vasopressin receptor 1A
AVPR V1a, AVPR1, V1aR
Autism, Hypertension, Schizophrenia

1156
Arginine vasopressin receptor 1B
AVPR3, V1bR, VPR3
Autism, Bipolar disorder, Bipolar depression, Mood disorder

1157
Arginine vasopressin receptor 2
ADHR, DI1, DIR, DIR3, NDI, NDI1, V2R
Arginine vasopressin resistance, Cardiomyopathy, Congestive heart failure, Neurogenic diabetes insipidus, Growth disorder, Heart failure, Nephrogenic diabetes insipidus

1158
Axonemal dynein light chain domain containing 1
C1orf125
Endocrine neoplasms, Kidney disease, Focal glomerulosclerosis, Nephrotic syndrome, Male infertility, Multiple sclerosis, Nephrotic syndrome, steroid-resistant, autosomal recessive, Retinal detachment, Schizophrenia, Steroid-resistant nephrotic syndrome, Testicular azoospermia

1159
Axin 1
AXIN, CMDOH, PPP1R49
Alzheimer disease, Androgenetic alopecia, Bone disease, Bone fracture, Hepatocellular carcinoma, Cardiovascular disease, Caudal duplication anomaly, Colorectal adenoma, Craniometadiaphyseal osteosclerosis with hip dysplasia, Metabolic syndrome, Osteoporosis, Diabetes mellitus type 2

1160
Axin 2
AXIL, ODCRCS
Dilated cardiomyopathy, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Craniosynostosis, Endometrial cancer, Endometriosis, Hirschsprung disease, Myocardial ischemia, Orofacial cleft, Tooth agenesis, Ventricular remodeling