GlyCosmos Portal

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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 **16051 - 16075** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	Disease Ontology
P34925	Tyrosine-protein kinase RYK	RYK JTK5A	Homo sapiens (human)	5
H7C4A2	Semaphorin 3F (Fragment)	SEMA3F	Homo sapiens (human)	1
A6NFC5	Transmembrane protein 235	TMEM235	Homo sapiens (human)	1
B5A958	Fibroblast growth factor receptor 1	FGFR1	Homo sapiens (human)	2
D5FWA4	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
F8R1D0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
Q86W61	VCAN protein	VCAN	Homo sapiens (human)	1
D7NNX7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
G1EPY7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
P59922	Putative olfactory receptor 2B8	OR2B8P OR2B8	Homo sapiens (human)	3
Q6PKH6	Dehydrogenase/reductase SDR family member 4-like 2	DHRS4L2 SDR25C3	Homo sapiens (human)	1
A0A0A7C5R8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A4P2SRK1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A0B4J266	T cell receptor alpha variable 41	TRAV41	Homo sapiens (human)	2
Q9NZN1	Interleukin-1 receptor accessory protein-like 1	IL1RAPL1 OPHN4	Homo sapiens (human)	6	B-cell lymphoma Bell's palsy Coffin-Lowry syndrome Klinefelter syndrome Marfan syndrome Meckel's diverticulum Patau syndrome X-linked adrenal hypoplasia congenita allergic asthma asthma attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome brain cancer breast cancer breast carcinoma cancer cardiovascular system disease chromosome Xp21 deletion syndrome clubfoot diffuse large B-cell lymphoma embryoma facial nerve disease facial paralysis heart disease hepatocellular carcinoma immune system disease intellectual disability intrinsic asthma learning disability liver cancer melanoma non-syndromic X-linked intellectual disability obesity obsolete ymphosarcoma placental insufficiency pyloric stenosis rheumatoid arthritis situs inversus skin melanoma syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy vitiligo
F5H522	Voltage-dependent L-type calcium channel subunit alpha	CACNA1C	Homo sapiens (human)	1
A0A1W2PPX5	Scavenger receptor class B member 2	SCARB2	Homo sapiens (human)	1
A2TJS3	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
D4HPK9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
A0A383S243	MHC class I antigen	HLA-C	Homo sapiens (human)	1
Q6ZMC9	Sialic acid-binding Ig-like lectin 15	SIGLEC15 CD33L3	Homo sapiens (human)	1	cancer embryoma osteoporosis
Q5JQS5	Olfactory receptor 2B11	OR2B11	Homo sapiens (human)	2
C0M117	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1
D4HPJ6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
A0A1C3PHK5	MHC class I antigen	HLA-B	Homo sapiens (human)	1

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