Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "A"

31 to 40 of 912 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
31	10095	ARPC1B	Actin related protein 2/3 complex subunit 1B	ARC41, IMD71, PLTEID, p40-ARC, p41-ARC	Lymphocytosis, Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease, Platelet-type bleeding disorder, Vasculitis
32	10097	ACTR2	Actin related protein 2	ARP2	Lung adenocarcinoma, Schizophrenia
33	10109	ARPC2	Actin related protein 2/3 complex subunit 2	ARC34, PNAS-139, PRO2446, p34-Arc	Ulcerative colitis
34	10120	ACTR1B	Actin related protein 1B	ARP1B, CTRN2, PC3	Colonic neoplasms, Colorectal cancer, Colorectal neoplasms
35	10121	ACTR1A	Actin related protein 1A	ARP1, Arp1A, CTRN1	Allergic rhinitis, Ulcerative colitis
36	10139	ARFRP1	ARF related protein 1	ARL18, ARP, Arp1	Breast cancer
37	10142	AKAP9	A-kinase anchoring protein 9	AKAP-9, AKAP350, AKAP450, CG-NAP, HYPERION, LQT11, MU-RMS-40.16A, PPP1R45, PRKA9, YOTIAO	Alzheimer disease, Arsenic encephalopathy, Atrioventricular block, Breast cancer, Breast carcinoma, Brugada syndrome, Bundle branch block, Colorectal cancer, Dermatologic disorders, Dysautonomia, Long qt syndrome, Paroxysmal ventricular tachycardia, Romano-ward syndrome, Sick sinus syndrome, Supraventricular tachycardia View all (3 more)
38	10149	ADGRG2	Adhesion G protein-coupled receptor G2	CBAVDX, EDDM6, GPR64, HE6, TM7LN2	Arthritis, Azoospermia, Absent vas deferens, Obstructive azoospermia, Oligospermia, Osteoarthrosis deformans
39	10157	AASS	Aminoadipate-semialdehyde synthase	LKR/SDH, LKRSDH, LORSDH	Alpha-aminoadipic semialdehyde deficiency disease, Anemia, Citrullinemia, Dwarfism, Ectopia lentis, Histidine transport defect, Hyperlysinemia, Impaired cognition, Spastic diplegia, Lysine alpha-ketoglutarate reductase deficiency disease, Mental retardation, Periodic hyperlysinemia, Saccharopinuria, Urogenital abnormalities
40	10159	ATP6AP2	ATPase H+ transporting accessory protein 2	(P)RR, APT6M8-9, ATP6IP2, ATP6M8-9, CDG2R, ELDF10, HT028, M8-9, MRXE, MRXSH, MSTP009, PRR, RENR, XMRE, XPDS	Agraphesthesia, Apraxia, Cerebellar atrophy, Cerebral atrophy, Cirrhosis, Hypoplasia of corpus callosum, Hypotonic seizures, Left ventricular hypertrophy, Mental retardation, Mental retardation, x-linked, Motor delay, Obesity, Parkinson disease, Parkinsonism-spasticity syndrome, x-linked, Scoliosis View all (2 more)

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