GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **2626 - 2650** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
214	activated leukocyte cell adhesion molecule	ALCAM
10973	activating signal cointegrator 1 complex subunit 3	ASCC3
466	activating transcription factor 1	ATF1
1386	activating transcription factor 2	ATF2
467	activating transcription factor 3	ATF3	prostate cancer pulmonary tuberculosis
468	activating transcription factor 4	ATF4	borna disease prostate carcinoma pulmonary venoocclusive disease
22809	activating transcription factor 5	ATF5
22926	activating transcription factor 6	ATF6
1388	activating transcription factor 6 beta	ATF6B
11016	activating transcription factor 7	ATF7
55729	activating transcription factor 7 interacting protein	ATF7IP
80063	activating transcription factor 7 interacting protein 2	ATF7IP2
26053	activator of transcription and developmental regulator AUTS2	AUTS2
94	activin A receptor like type 1	ACVRL1
90	activin A receptor type 1	ACVR1
91	activin A receptor type 1B	ACVR1B
92	activin A receptor type 2A	ACVR2A
93	activin A receptor type 2B	ACVR2B
23394	activity dependent neuroprotector homeobox	ADNP
91452	acyl-CoA binding domain containing 5	ACBD5
84129	acyl-CoA dehydrogenase family member 11	ACAD11
28976	acyl-CoA dehydrogenase family member 9	ACAD9
33	acyl-CoA dehydrogenase long chain	ACADL ACAD4 LCAD long-chain acyl-CoA dehydrogenase	Pearson syndrome atrial fibrillation cancer cardiomyopathy chronic kidney disease embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fibromyalgia hepatocellular carcinoma hypertrophic cardiomyopathy hypoglycemia liver cancer liver carcinoma myositis nuclear type mitochondrial complex I deficiency 20 steatotic liver disease urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency
34	acyl-CoA dehydrogenase medium chain	ACADM ACAD1 MCAD MCADH medium-chain acyl-CoA dehydrogenase	D-bifunctional protein deficiency Reye syndrome brain edema breast cancer breast carcinoma cancer carnitine palmitoyltransferase I deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure cystinuria diarrhea disease of metabolism distal arthrogryposis epilepsy familial periodic paralysis galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis hydrocephalus hypoglycemia hypoglycemic coma inherited metabolic disorder isolated elevated serum creatine phosphokinase levels lactic acidosis large intestine cancer liver disease long QT syndrome medium chain acyl-CoA dehydrogenase deficiency metabolic dysfunction-associated steatotic liver disease myopathy neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma obesity papillary renal cell carcinoma perinatal necrotizing enterocolitis phenylketonuria pseudosarcomatous fibromatosis psoriatic arthritis renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sick sinus syndrome steatotic liver disease sudden infant death syndrome systemic primary carnitine deficiency disease urea cycle disorder visual epilepsy
35	acyl-CoA dehydrogenase short chain	ACADS ACAD3 SCAD	Bell's palsy Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Stevens-Johnson syndrome X-linked Aarskog syndrome alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bipolar disorder cancer cardiomyopathy chondrodysplasia-pseudohermaphroditism syndrome chronic kidney disease congestive heart failure coronary artery disease embryoma endomyocardial fibrosis epilepsy erythema multiforme facial nerve disease facial paralysis familial periodic paralysis hepatocellular carcinoma hypertrophic cardiomyopathy liver cancer medium chain acyl-CoA dehydrogenase deficiency microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II myopathy nutmeg liver pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder scoliosis short chain acyl-CoA dehydrogenase deficiency visual epilepsy

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