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 **16026 - 16050** 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
Q8NHS4	Clathrin heavy chain linker domain-containing protein 1	CLHC1 C2orf63	Homo sapiens (human)	0	1
O14967	Calmegin	CLGN	Homo sapiens (human)	1	2	breast cancer breast carcinoma prostate cancer prostate carcinoma seminoma testicular cancer testicular germ cell cancer testis seminoma
Q8IZS7	Putative C-type lectin-like domain family 1	CLECL1P CLECL1 DCAL1	Homo sapiens (human)	3	0
Q6UXN8	C-type lectin domain family 9 member A	CLEC9A	Homo sapiens (human)	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
Q9BXN2	C-type lectin domain family 7 member A	CLEC7A BGR CLECSF12 DECTIN1	Homo sapiens (human)	3	2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Behcet's disease Bloch-Sulzberger syndrome Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Pick's disease Reye syndrome acquired hyperkeratosis acute myeloid leukemia adult-onset Still's disease allergic asthma amyloidosis angular cheilitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aspergillosis asthma atherosclerosis atopic dermatitis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome bacterial infectious disease bacterial sepsis black piedra blastomycosis cancer candidiasis cerebral degeneration cheilitis cholesteatoma chromoblastomycosis chronic mucocutaneous candidiasis chronic obstructive pulmonary disease chronic ulcer of skin coccidioidomycosis colitis congenital intrinsic factor deficiency coronary artery disease cryptococcosis cutaneous leishmaniasis cystic fibrosis dermatitis dermatomycosis dermatophytosis diverticulitis embryoma epilepsy exanthem fungal infectious disease gastroenteritis granuloma annulare hepatitis B hepatitis hepatocellular carcinoma histoplasmosis hypomelanosis of Ito ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intrinsic asthma keratitis keratoconjunctivitis lip disease liver cancer liver carcinoma liver cirrhosis lupus nephritis male infertility mycotic corneal ulcer nutmeg liver obesity oral candidiasis osteoarthritis pancreatic cancer pancreatic carcinoma paracoccidioidomycosis parapsoriasis parasitic helminthiasis infectious disease patent ductus arteriosus pneumocystosis pneumonia polyp of middle ear psoriasis pustulosis of palm and sole rheumatoid arthritis shigellosis sporotrichosis superficial mycosis systemic lupus erythematosus tinea favosa tuberculosis ulcerative colitis urinary tract obstruction vasculitis visual epilepsy vulvovaginal candidiasis white piedra
Q6EIG7	C-type lectin domain family 6 member A	CLEC6A CLECSF10 DECTIN2	Homo sapiens (human)	2	0	Kawasaki disease acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer candidiasis cholesteatoma coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis dermatomycosis dermatophytosis embryoma fungal infectious disease myocardial infarction pneumocystosis pneumonia polyp of middle ear rheumatoid arthritis silent myocardial infarction superficial mycosis tinea favosa tuberculosis vasculitis
Q9NY25	C-type lectin domain family 5 member A	CLEC5A CLECSF5 MDL1	Homo sapiens (human)	4	0	Japanese encephalitis Mycoplasma pneumoniae pneumonia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bone osteosarcoma brain glioblastoma multiforme central nervous system cancer cholesteatoma dengue disease dengue hemorrhagic fever giant cell glioblastoma glioblastoma gliosarcoma high grade glioma mixed glioma osteoarthritis osteosarcoma polyp of middle ear viral infectious disease yellow fever
Q9H2X3	C-type lectin domain family 4 member M	CLEC4M CD209L CD209L1 CD299	Homo sapiens (human)	2	0
Q6UXB4	C-type lectin domain family 4 member G	CLEC4G	Homo sapiens (human)	2	0	Ebola hemorrhagic fever basal cell carcinoma breast cancer breast carcinoma hepatocellular carcinoma liver cancer
Q8N1N0	C-type lectin domain family 4 member F	CLEC4F CLECSF13	Homo sapiens (human)	8	0
Q9ULY5	C-type lectin domain family 4 member E	CLEC4E CLECSF9 MINCLE	Homo sapiens (human)	2	0	acute myocardial infarction allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis coronary thrombosis depressive disorder dysthymic disorder intrinsic asthma keratitis keratoconjunctivitis major depressive disorder melancholic depression multiple sclerosis mycotic corneal ulcer myocardial infarction neurotic disorder obsolete melancholia pulmonary tuberculosis rheumatoid arthritis silent myocardial infarction tuberculosis tuberculous pneumothorax
Q8WXI8	C-type lectin domain family 4 member D	CLEC4D CLECSF8 MCL	Homo sapiens (human)	3	0
Q8WTT0	C-type lectin domain family 4 member C	CLEC4C BDCA2 CLECSF11 CLECSF7 DLEC HECL	Homo sapiens (human)	3	0
Q9UMR7	C-type lectin domain family 4 member A	CLEC4A CLECSF6 DCIR LLIR	Homo sapiens (human)	1	0
P05452	Tetranectin	CLEC3B TNA	Homo sapiens (human)	1	0
Q9UHP7	C-type lectin domain family 2 member D	CLEC2D CLAX LLT1 OCIL	Homo sapiens (human)	2	0
Q92478	C-type lectin domain family 2 member B	CLEC2B AICL CLECSF2 IFNRG1	Homo sapiens (human)	5	1	cancer hepatocellular carcinoma liver cancer
Q6UVW9	C-type lectin domain family 2 member A	CLEC2A KACL	Homo sapiens (human)	3	0
Q9P126	C-type lectin domain family 1 member B	CLEC1B CLEC2	Homo sapiens (human)	3	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Evans' syndrome Marfan syndrome Pick's disease Reye syndrome adult respiratory distress syndrome androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autoimmune thrombocytopenic purpura bacterial sepsis blood coagulation disease cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma gallbladder disease hematopoietic system disease hemolytic-uremic syndrome hepatocellular carcinoma liver cancer liver disease lung benign neoplasm melanoma newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver obsolete inherited blood coagulation disease papillary renal cell carcinoma pneumonia renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma situs inversus skin melanoma split hand-foot malformation 1 stomach cancer stomach carcinoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thrombotic thrombocytopenic purpura tuberous sclerosis type 2 diabetes mellitus viral infectious disease
Q8NC01	C-type lectin domain family 1 member A	CLEC1A CLEC1	Homo sapiens (human)	2	0	aspergillosis black piedra coccidioidomycosis histoplasmosis sporotrichosis superficial mycosis white piedra
Q6UXS0	C-type lectin domain family 19 member A	CLEC19A	Homo sapiens (human)	1	0
Q8NCF0	C-type lectin domain family 18 member C	CLEC18C MRLP3	Homo sapiens (human)	1	0
Q6UXF7	C-type lectin domain family 18 member B	CLEC18B MRLP1	Homo sapiens (human)	1	0	acquired immunodeficiency syndrome cancer embryoma giant cell glioblastoma glioblastoma high grade glioma
A5D8T8	C-type lectin domain family 18 member A	CLEC18A MRLP2	Homo sapiens (human)	2	1
Q6ZS10	C-type lectin domain family 17, member A	CLEC17A	Homo sapiens (human)	3	0	Richter's syndrome chronic lymphocytic leukemia

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