GlyCosmos Portal

Displaying entries **10001 - 10025** of **10109** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
51554	atypical chemokine receptor 4	ACKR4
57007	atypical chemokine receptor 3	ACKR3
1238	atypical chemokine receptor 2	ACKR2
2532	atypical chemokine receptor 1 (Duffy blood group)	ACKR1	Plasmodium vivax malaria malaria
22985	apoptotic chromatin condensation inducer 1	ACIN1
43	acetylcholinesterase (Yt blood group)	ACHE Yt blood group	Alzheimer's disease cannabis dependence drug dependence epilepsy heroin dependence myasthenia gravis subacute delirium
55331	alkaline ceramidase 3	ACER3 APHC FLJ11238 alkaline phytoceramidase
340485	alkaline ceramidase 2	ACER2 ALKCDase2 FLJ41587
125981	alkaline ceramidase 1	ACER1
59272	angiotensin converting enzyme 2	ACE2	COVID-19 avian influenza cerebral malaria diabetic retinopathy hypertension pulmonary hypertension respiratory syncytial virus infectious disease severe acute respiratory syndrome
1636	angiotensin I converting enzyme	ACE ACE1 CD143 peptidyl-dipeptidase A	Behcet's disease COVID-19 Coronavirus infectious disease Fabry disease IgA glomerulonephritis IgA vasculitis allergic disease anemia ankylosing spondylitis aspiration pneumonia asthma atrial fibrillation breast cancer cerebral infarction chronic obstructive pulmonary disease coronary artery disease diabetic retinopathy diastolic heart failure end stage renal disease familial Mediterranean fever gallbladder adenocarcinoma heart valve disease hepatitis A hepatocellular carcinoma hypertension leukemia liver cirrhosis lung cancer mitral valve disease mitral valve prolapse multiple myeloma myocardial infarction nephritis non-arteritic anterior ischemic optic neuropathy obstructive sleep apnea pneumonia polycythemia pre-eclampsia proteinuria sarcoidosis stomach cancer subacute sclerosing panencephalitis toxic shock syndrome type 1 diabetes mellitus type 2 diabetes mellitus
65057	ACD shelterin complex subunit and telomerase recruitment factor	ACD	autosomal dominant dyskeratosis congenita 6
91452	acyl-CoA binding domain containing 5	ACBD5	retinal dystrophy with leukodystrophy
39	acetyl-CoA acetyltransferase 2	ACAT2 Acetyl-CoA acetyltransferase, cytosolic acetoacetyl Coenzyme A thiolase	coronary artery disease
38	acetyl-CoA acetyltransferase 1	ACAT1 THIL acetoacetyl Coenzyme A thiolase	beta-ketothiolase deficiency carbohydrate metabolic disorder
23527	ArfGAP with coiled-coil, ankyrin repeat and PH domains 2	ACAP2
9744	ArfGAP with coiled-coil, ankyrin repeat and PH domains 1	ACAP1
176	aggrecan	ACAN CSPGCP aggrecan proteoglycan	spondyloepiphyseal dysplasia Kimberley type
37	acyl-CoA dehydrogenase very long chain	ACADVL ACAD6 LCACD VLCAD	very long chain acyl-CoA dehydrogenase deficiency
36	acyl-CoA dehydrogenase short/branched chain	ACADSB ACAD7 SBCAD
35	acyl-CoA dehydrogenase short chain	ACADS ACAD3 SCAD	alcohol use disorder short chain acyl-CoA dehydrogenase deficiency
34	acyl-CoA dehydrogenase medium chain	ACADM ACAD1 MCAD MCADH medium-chain acyl-CoA dehydrogenase	medium chain acyl-CoA dehydrogenase deficiency
33	acyl-CoA dehydrogenase long chain	ACADL ACAD4 LCAD long-chain acyl-CoA dehydrogenase
28976	acyl-CoA dehydrogenase family member 9	ACAD9	nuclear type mitochondrial complex I deficiency 20
84129	acyl-CoA dehydrogenase family member 11	ACAD11

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