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
561 to 570 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

561
AMMECR1 like
-
Alzheimer disease

562
Amnion associated transmembrane protein
IGS2, PRO1028, amnionless
Megaloblastic anemia, Anxiety disorder, Edema, Extravasation of diagnostic and therapeutic materials, Imerslund-grasbeck syndrome, Kidney failure, Post-traumatic stress disorder, Diabetes mellitus type 2, Vitamin b deficiency

563
Angiomotin
-
Brain neoplasms

564
Angiomotin like 1
CFCHS, JEAP
Basal cell carcinoma, Cleft lip and palate, Craniofaciocardiohepatic syndrome, Glioma, Auricle malformation, Non-melanoma skin carcinoma, Orofacial cleft, Tethered cord syndrome

565
Adenosine monophosphate deaminase 1
MAD, MADA, MMDD
Myoadenylate deaminase deficiency, Autism, Ischemic heart disease, Congestive heart failure, Coronary artery disease, Heart failure, Hyperlipoproteinemia, Ovarian epithelial cancer, Myocardial ischemia, Myopathy, Ovarian cancer

566
Adenosine monophosphate deaminase 2
AMPD, PCH9, SPG63
Autoimmune thrombocytopenic purpura, Spastic paraplegia, Breast cancer, Congenital brain malformation, Congenital hypoplasia of part of brain, Congenital neurologic anomalies, Estrogen-receptor negative breast cancer, Global developmental delay, Hydranencephaly, Intellectual developmental disorder, Lissencephaly, Macrogyria, Microgyria, Pontocerebellar hypoplasia, Spastic ataxia
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567
Adenosine monophosphate deaminase 3
-
Myoadenylate deaminase deficiency, Atrial fibrillation, Bipolar disorder, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Melanoma, Erythrocyte amp deaminase deficiency, Hemorrhoid, Hypertension, Major depressive disorder, Nephrolithiasis, Osteoarthritis, Scoliosis

568
Amphiphysin
AMPH1
Scoliosis, Small vessel stroke

569
Aminomethyltransferase
GCE, GCE2, GCST, GCVT, NKH
Glycine encephalopathy, Hyperglycemia

570
Amelotin
AI3B, UNQ689
Amelogenesis imperfecta, Diabetic neuropathy, Esophageal squamous cell carcinoma, Scoliosis, Uterine polyp