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 **16876 - 16900** 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
A0A4Z1	CADM1 protein	CADM1	Homo sapiens (human)	3	0
F5H125	Cell adhesion molecule 1 (Fragment)	CADM1	Homo sapiens (human)	2	0
H1ZZW4	CADM1 protein (Fragment)	CADM1	Homo sapiens (human)	1	0
A0A087X0T8	Cell adhesion molecule 1	CADM1	Homo sapiens (human)	3	0
X5D8W0	Cell adhesion molecule 1 isoform D (Fragment)	CADM1	Homo sapiens (human)	3	0
Q9BY67	Cell adhesion molecule 1	CADM1 IGSF4 IGSF4A NECL2 SYNCAM TSLC1	Homo sapiens (human)	12	47
P27708	Multifunctional protein CAD	CAD	Homo sapiens (human)	5	1
Q9HB71	Calcyclin-binding protein	CACYBP S100A6BP SIP	Homo sapiens (human)	1	1
Q86Y37	CDK2-associated and cullin domain-containing protein 1	CACUL1 C10orf46 CAC1	Homo sapiens (human)	4	1
Q8WUQ7	Splicing factor Cactin	CACTIN C19orf29	Homo sapiens (human)	0	1
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
O00305	Voltage-dependent L-type calcium channel subunit beta-4	CACNB4 CACNLB4	Homo sapiens (human)	0	1
Q08289	Voltage-dependent L-type calcium channel subunit beta-2	CACNB2 CACNLB2 MYSB	Homo sapiens (human)	2	1
Q02641	Voltage-dependent L-type calcium channel subunit beta-1	CACNB1 CACNLB1	Homo sapiens (human)	0	1
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
A0A7P0T8M7	Voltage-dependent L-type calcium channel subunit alpha	CACNA1S	Homo sapiens (human)	2	0
A0A7P0TBJ5	Voltage-dependent L-type calcium channel subunit alpha	CACNA1S	Homo sapiens (human)	2	0
B1ALM3	Voltage-dependent L-type calcium channel subunit alpha	CACNA1S	Homo sapiens (human)	2	0

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