GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3201 - 3225** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
9620	cadherin EGF LAG seven-pass G-type receptor 1	CELSR1
1952	cadherin EGF LAG seven-pass G-type receptor 2	CELSR2
1951	cadherin EGF LAG seven-pass G-type receptor 3	CELSR3
79974	cadherin like and PC-esterase domain containing 1	CPED1
64072	cadherin related 23	CDH23
92211	cadherin related family member 1	CDHR1
54825	cadherin related family member 2	CDHR2
222256	cadherin related family member 3	CDHR3
389118	cadherin related family member 4	CDHR4
53841	cadherin related family member 5	CDHR5
793	calbindin 1	CALB1
23523	calcineurin binding protein 1	CABIN1
799	calcitonin receptor	CALCR
10203	calcitonin receptor like receptor	CALCRL
796	calcitonin related polypeptide alpha	CALCA
797	calcitonin related polypeptide beta	CALCB
124583	calcium activated nucleotidase 1	CANT1 SCAN-1 SHAPY Soluble Ca-Activated Nucleotidase, isozyme 1 apyrase 1 homolog (C. lectularius)
26256	calcium binding tyrosine phosphorylation regulated	CABYR
8618	calcium dependent secretion activator	CADPS
10523	calcium homeostasis endoplasmic reticulum protein	CHERP
255022	calcium homeostasis modulator 1	CALHM1
119395	calcium homeostasis modulator 3	CALHM3
846	calcium sensing receptor	CASR
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
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

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