GlyCosmos Portal

Displaying entries **13501 - 13525** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q9UK85	Dickkopf-like protein 1	DKKL1 SGY1	2	0
Q9Y2J4	Angiomotin-like protein 2	AMOTL2 KIAA0989	2	2
Q9H2H9	Sodium-coupled neutral amino acid symporter 1	SLC38A1 ATA1 NAT2 SAT1 SNAT1	2	0
Q8WV99	AN1-type zinc finger protein 2B	ZFAND2B AIRAPL	2	1
Q9NTU7	Cerebellin-4	CBLN4 CBLNL1	2	4
Q8N3R9	Protein PALS1	PALS1 MPP5	2	2
A0A087X0D5	Pro-cathepsin H	CTSH	2	0
P07355	Annexin A2	ANXA2 ANX2 ANX2L4 CAL1H LPC2D	2	2
P50219	Motor neuron and pancreas homeobox protein 1	MNX1 HLXB9	2	1
Q6UXN8	C-type lectin domain family 9 member A	CLEC9A	2	0	acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease herpes simplex human immunodeficiency virus infectious disease influenza leprosy pneumonia primary immunodeficiency disease tuberculosis viral infectious disease
Q0D2K2	Kelch-like protein 30	KLHL30	2	1
Q9C0K1	Metal cation symporter ZIP8	SLC39A8 BIGM103 ZIP8	2	2	Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute chest syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood androgen insensitivity syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy astigmatism atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autonomic neuropathy bacterial sepsis breast cancer breast carcinoma cancer central nervous system disease cerebral infarction cerebrovascular disease childhood leukemia colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type IIn congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease craniosynostosis dermatitis diabetes mellitus diabetic ketoacidosis dissociated nystagmus dystonia epilepsy essential hypertension focal hand dystonia generalized dystonia hemochromatosis hydrocephalus hyperopia hypertension hypertropia idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability iron metabolism disease kwashiorkor large intestine cancer learning disability left ventricular noncompaction leukemia macrocytic anemia marasmus mechanical strabismus mitochondrial metabolism disease mitochondrial myopathy nervous system disease neuroblastoma nicotine dependence nutrition disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus protein-energy malnutrition pulmonary tuberculosis schizophrenia sensorineural hearing loss spontaneous ocular nystagmus strabismus systemic lupus erythematosus tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis visual epilepsy
Q8ND24	RING finger protein 214	RNF214	2	1
Q3ZCQ3	Membrane protein FAM174B	FAM174B	2	3
Q15545	Transcription initiation factor TFIID subunit 7	TAF7 TAF2F TAFII55	2	1
A0A087WYZ4	Glycoprotein hormones alpha chain	CGA	2	0
Q9NZJ0	Denticleless protein homolog	DTL CDT2 CDW1 DCAF2 L2DTL RAMP	2	2
Q15818	Neuronal pentraxin-1	NPTX1	2	1
Q49A17	Polypeptide N-acetylgalactosaminyltransferase-like 6	GALNTL6 GALNT17	2	0	nicotine dependence
I3L192	Basigin (Ok blood group) (Fragment)	BSG	2	0
O96019	Actin-like protein 6A	ACTL6A BAF53 BAF53A INO80K	2	1
O95996	Adenomatous polyposis coli protein 2	APC2 APCL	2	2
Q9UBY0	Sodium/hydrogen exchanger 2	SLC9A2 NHE2	2	1
Q8IWM0	Apolipoprotein J (Fragment)	CLU	2	0
Q6ZQN7	Solute carrier organic anion transporter family member 4C1	SLCO4C1 OATP4C1 OATPX SLC21A20	2	4

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