GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8901 - 8925** of **9988** in total

« First

‹ Prev

…

353

354

355

356

357

358

359

360

361

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
796	calcitonin related polypeptide alpha	CALCA
793	calbindin 1	CALB1
8618	calcium dependent secretion activator	CADPS
199731	cell adhesion molecule 4	CADM4
57863	cell adhesion molecule 3	CADM3
253559	cell adhesion molecule 2	CADM2
23705	cell adhesion molecule 1	CADM1
790	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	CAD GATD4
27101	calcyclin binding protein	CACYBP
143384	CDK2 associated cullin domain 1	CACUL1
58509	cactin, spliceosome C complex subunit	CACTIN
59283	calcium voltage-gated channel auxiliary subunit gamma 8	CACNG8
27092	calcium voltage-gated channel auxiliary subunit gamma 4	CACNG4
10369	calcium voltage-gated channel auxiliary subunit gamma 2	CACNG2
786	calcium voltage-gated channel auxiliary subunit gamma 1	CACNG1
783	calcium voltage-gated channel auxiliary subunit beta 2	CACNB2
782	calcium voltage-gated channel auxiliary subunit beta 1	CACNB1
93589	calcium voltage-gated channel auxiliary subunit alpha2delta 4	CACNA2D4 alpha2delta-4	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness retinal cone dystrophy 4 spontaneous ocular nystagmus strabismus
55799	calcium voltage-gated channel auxiliary subunit alpha2delta 3	CACNA2D3 HSA272268 alpha2delta-3	acute myeloid leukemia anemia breast cancer breast carcinoma cancer carcinoma central nervous system cancer deficiency anemia embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gliosarcoma heart conduction disease high grade glioma hypochromic anemia lung squamous cell carcinoma macrocytic anemia microcytic anemia mixed glioma nasopharynx carcinoma nicotine dependence prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia stomach cancer stomach carcinoma uterine corpus cancer
9254	calcium voltage-gated channel auxiliary subunit alpha2delta 2	CACNA2D2 KIAA0558 alpha2delta-2 gene 26	absence epilepsy agnosia alternating hemiplegia of childhood autonomic neuropathy bipolar I disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebellar ataxia cerebellar disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 21 dissociated nystagmus embryoma epilepsy hypertropia idiopathic generalized epilepsy large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maple syrup urine disease mechanical strabismus nasopharynx carcinoma nervous system disease ophthalmoplegia pathologic nystagmus primary cutaneous amyloidosis prostate cancer prostate carcinoma sensorineural hearing loss sick sinus syndrome spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability type 10
781	calcium voltage-gated channel auxiliary subunit alpha2delta 1	CACNA2D1 alpha2delta-1 lncRNA-N3	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome West syndrome Williams-Beuren syndrome acute myeloid leukemia amelogenesis imperfecta type 1G atrial fibrillation atrioventricular block azoospermia brain infarction cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder developmental and epileptic encephalopathy 110 embryoma epilepsy essential hypertension glaucoma hepatocellular carcinoma hypertension idiopathic scoliosis intellectual disability large intestine cancer learning disability liver cancer major depressive disorder malignant hyperthermia melancholic depression neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia primary open angle glaucoma short QT syndrome sick sinus syndrome stomach cancer stomach carcinoma supravalvular aortic stenosis uveal melanoma
779	calcium voltage-gated channel subunit alpha1 S	CACNA1S
8911	calcium voltage-gated channel subunit alpha1 I	CACNA1I
8912	calcium voltage-gated channel subunit alpha1 H	CACNA1H
8913	calcium voltage-gated channel subunit alpha1 G	CACNA1G

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements