Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

861 to 870 of 912 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
861	91074	ANKRD30A	Ankyrin repeat domain 30A	NY-BR-1	Ankylosing spondylitis, Arthritis, Autoimmune diseases, Autoimmune thyroiditis, Breast cancer, Celiac disease, Common variable immunodeficiency, Crohn disease, Diabetes mellitus, Lupus erythematosus, Psoriasis, Ulcerative colitis
862	9114	ATP6V0D1	ATPase H+ transporting V0 subunit d1	ATP6D, ATP6DV, P39, VATX, VMA6, VPATPD	Age-related macular degeneration
863	9131	AIFM1	Apoptosis inducing factor mitochondria associated 1	AIF, AUNX1, CMT2D, CMTX4, COWCK, COXPD6, DFNX5, NADMR, NAMSD, PDCD8, SEMDHL	Akinetic-rigid variant of huntington disease, Auditory neuropathy, Autoimmune diabetes, Cerebral atrophy, Charcot-marie-tooth disease, x-linked, Combined oxidative phosphorylation deficiency, Cowchock syndrome, Deafness, Developmental delay, Developmental regression, Diabetes mellitus, Brittle diabetes mellitus, Dyssomnia, Hearing loss, Hereditary sensory and autonomic neuropathy with deafness, x-linked View all (19 more)
864	9138	ARHGEF1	Rho guanine nucleotide exchange factor 1	GEF1, IMD62, LBCL2, LSC, P115-RHOGEF, SUB1.5	Bronchiectasis, Colorectal cancer, Immune thrombocytopenic purpura
865	91526	ANKRD44	Ankyrin repeat domain 44	ARSB, PP6-ARS-B	Aortic aneurysm, Intracranial aneurysm, Lupus erythematosus, Prostate cancer
866	91647	ATPAF2	ATP synthase mitochondrial F1 complex assembly factor 2	ATP12, ATP12p, LP3663, MC5DN1	Coronary artery disease, Cryptorchidism, Developmental delay, Dwarfism, Hypertrophic cardiomyopathy, Hypospadias, Isolated atp synthase deficiency, Microcephaly, Mitochondrial complex deficiency, Mitochondrial diseases
867	9179	AP4M1	Adaptor related protein complex 4 subunit mu 1	CPSQ3, MU-4, MU-ARP2, SPG50	Alzheimer disease, Brain atrophy, Cerebellar atrophy, Cerebral cortical atrophy, Cerebral palsy, Congenital clubfoot, Developmental dysplasia of the hip, Congenital genu recurvatum, Developmental delay, Dwarfism, High palate, Hypoplasia of corpus callosum, Mental retardation, Macrostomia, Malocclusion View all (8 more)
868	91801	ALKBH8	AlkB homolog 8, tRNA methyltransferase	ABH8, MRT71, TRM9, TRMT9, TRMT9A	Attention deficit hyperactivity disorder, Breast cancer, Mammary neoplasms, Breast carcinoma, Cryptorchidism, Developmental delay, Macrocephaly, Macrotia, Marfan syndrome, Mental retardation, Narcolepsy, Non-syndromic intellectual disability, Penis agenesis, Stereotyped behavior
869	9181	ARHGEF2	Rho/Rac guanine nucleotide exchange factor 2	GEF, GEF-H1, GEFH1, LFP40, Lfc, NEDMHM, P40	Amyotrophic lateral sclerosis, Astigmatism, High palate, Mental retardation, Microcephaly, Motor delay, Neurodevelopmental disorder with midbrain and hindbrain malformations, Nystagmus, Ptosis, Strabismus
870	92	ACVR2A	Activin A receptor type 2A	ACTRII, ACVR2	Gastric cancer, Gout, Gouty arthritis

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