Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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"

771 to 780 of 912 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
771	80832	APOL4	Apolipoprotein L4	APOL-IV, APOLIV	Delusions, Hallucinations, Schizophrenia
772	8086	AAAS	Aladin WD repeat nucleoporin	AAA, AAASb, ADRACALA, ADRACALIN, ALADIN, GL003	Achalasia, Alacrima, Congenital alacrima, Congenital coloboma of iris, Developmental delay, Developmental regression, Dwarfism, Dysarthria, Dysautonomia, Esophageal stricture, Glucocorticoid deficiency with achalasia, Hearing loss, Hypopituitarism, Mental retardation, Microcephaly View all (7 more)
773	8092	ALX1	ALX homeobox 1	CART1, FND3, HEL23	Absent eyebrow, Agenesis of corpus callosum, Brachycephaly, Brachydactyly, Cataract, Clinodactyly, Congenital epicanthus, Frontonasal dysplasia, Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome, Hearing loss, Hypoplasia of the maxilla, Lipoma of corpus callosum, Mental retardation, Microphthalmos, Parietal foramina, Ptosis, Tetralogy of fallot View all (2 more)
774	81	ACTN4	Actinin alpha 4	ACTININ-4, FSGS, FSGS1	Anaplastic carcinoma, Anemia, Carcinoma, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glomerular hyalinosis, Glomerulosclerosis, Hyperlipidemia, Hypertension, Hypoalbuminemia, Nephritis
775	8120	AP3B2	Adaptor related protein complex 3 subunit beta 2	DEE48, EIEE48, NAPTB	Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Gastroesophageal reflux disease, Hypodontia, Mental retardation, Microcephaly, Non-specifi epileptic encephalopathy, Nystagmus, Optic atrophy View all (3 more)
776	8125	ANP32A	Acidic nuclear phosphoprotein 32 family member A	C15orf1, HPPCn, I1PP2A, LANP, MAPM, PHAP1, PHAPI, PP32	Colorectal cancer, Colorectal neoplasms, Lung adenocarcinoma
777	81575	APOLD1	Apolipoprotein L domain containing 1	BDVAS, VERGE	Cardiovascular diseases, Prostate cancer
778	8165	AKAP1	A-kinase anchoring protein 1	AKAP, AKAP121, AKAP149, AKAP84, D-AKAP1, PPP1R43, PRKA1, SAKAP84, TDRD17	Obesity
779	81693	AMN	Amnion associated transmembrane protein	IGS2, PRO1028, amnionless	Anemia, Cobalamin deficiency, Dementia, Imerslund-grasbeck syndrome, Kidney failure, Acute kidney insufficiency
780	81792	ADAMTS12	ADAM metallopeptidase with thrombospondin type 1 motif 12	PRO4389	Schizophrenia

«««...76 777879 80...»»»