GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **626 - 650** of **18496** in total

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UniProt ID	Protein Name ▼	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q7Z3S7	Voltage-dependent calcium channel subunit alpha-2/delta-4	CACNA2D4	Homo sapiens (human)	3	1	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 spontaneous ocular nystagmus strabismus
Q8IZS8	Voltage-dependent calcium channel subunit alpha-2/delta-3	CACNA2D3	Homo sapiens (human)	5	0	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 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
Q9NY47	Voltage-dependent calcium channel subunit alpha-2/delta-2	CACNA2D2 KIAA0558	Homo sapiens (human)	11	6	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
P54289	Voltage-dependent calcium channel subunit alpha-2/delta-1	CACNA2D1 CACNL2A CCHL2A MHS3	Homo sapiens (human)	17	53	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 cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder 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
Q8WXS5	Voltage-dependent calcium channel gamma-8 subunit	CACNG8 CACNG6	Homo sapiens (human)	2	1
Q9UBN1	Voltage-dependent calcium channel gamma-4 subunit	CACNG4	Homo sapiens (human)	2	0
O60359	Voltage-dependent calcium channel gamma-3 subunit	CACNG3	Homo sapiens (human)	0	1
Q9Y698	Voltage-dependent calcium channel gamma-2 subunit	CACNG2	Homo sapiens (human)	1	1
Q06432	Voltage-dependent calcium channel gamma-1 subunit	CACNG1 CACNLG	Homo sapiens (human)	2	0
Q8N350	Voltage-dependent calcium channel beta subunit-associated regulatory protein	CBARP C19orf26	Homo sapiens (human)	1	0
Q9Y277	Voltage-dependent anion-selective channel protein 3	VDAC3	Homo sapiens (human)	2	2
P45880	Voltage-dependent anion-selective channel protein 2	VDAC2	Homo sapiens (human)	4	2
P21796	Voltage-dependent anion-selective channel protein 1	VDAC1 VDAC	Homo sapiens (human)	3	3
Q9P0X4	Voltage-dependent T-type calcium channel subunit alpha-1I	CACNA1I KIAA1120	Homo sapiens (human)	7	1
O95180	Voltage-dependent T-type calcium channel subunit alpha-1H	CACNA1H	Homo sapiens (human)	9	3
O43497	Voltage-dependent T-type calcium channel subunit alpha-1G	CACNA1G KIAA1123	Homo sapiens (human)	8	0
Q15878	Voltage-dependent R-type calcium channel subunit alpha-1E	CACNA1E CACH6 CACNL1A6	Homo sapiens (human)	5	2
O00555	Voltage-dependent P/Q-type calcium channel subunit alpha-1A	CACNA1A CACH4 CACN3 CACNL1A4	Homo sapiens (human)	1	1
Q9NS89	Voltage-dependent P/Q-type calcium channel subunit alpha (Fragment)	CACNA1A	Homo sapiens (human)	1	0
A0A1B0GTW2	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Homo sapiens (human)	1	0
A0A1B0GTI4	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Homo sapiens (human)	1	0
B5TYJ1	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Homo sapiens (human)	1	0
A0A1B0GTN7	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Homo sapiens (human)	1	0
A0A590UJK2	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Homo sapiens (human)	1	0
A0A1B0GU74	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	Homo sapiens (human)	1	0

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