GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **3801 - 3825** of **9988** in total

« First

‹ Prev

…

149

150

151

152

153

154

155

156

157

…

Next ›

Last »
Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
1300	collagen type X alpha 1 chain	COL10A1
1301	collagen type XI alpha 1 chain	COL11A1
1302	collagen type XI alpha 2 chain	COL11A2
1303	collagen type XII alpha 1 chain	COL12A1
7373	collagen type XIV alpha 1 chain	COL14A1
1310	collagen type XIX alpha 1 chain	COL19A1
1306	collagen type XV alpha 1 chain	COL15A1
1307	collagen type XVI alpha 1 chain	COL16A1
1308	collagen type XVII alpha 1 chain	COL17A1
80781	collagen type XVIII alpha 1 chain	COL18A1
57642	collagen type XX alpha 1 chain	COL20A1
81578	collagen type XXI alpha 1 chain	COL21A1
169044	collagen type XXII alpha 1 chain	COL22A1
91522	collagen type XXIII alpha 1 chain	COL23A1
255631	collagen type XXIV alpha 1 chain	COL24A1
84570	collagen type XXV alpha 1 chain	COL25A1
136227	collagen type XXVI alpha 1 chain	COL26A1
85301	collagen type XXVII alpha 1 chain	COL27A1
340267	collagen type XXVIII alpha 1 chain	COL28A1
1400	collapsin response mediator protein 1	CRMP1
10584	collectin subfamily member 10	COLEC10 CL-10 CL-L1	3MC syndrome 3 3MC syndrome Klippel-Feil syndrome Laron syndrome Richter's syndrome achondroplasia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia allergic asthma asthma basal cell carcinoma blepharophimosis cancer carcinoma chronic lymphocytic leukemia cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism essential thrombocythemia hepatocellular carcinoma humeroradial synostosis intellectual disability isolated cleft palate learning disability liver cancer lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma omphalocele ptosis radioulnar synostosis scoliosis sebaceous carcinoma sensorineural hearing loss spina bifida occulta spondylolisthesis sweat gland cancer umbilical hernia
78989	collectin subfamily member 11	COLEC11 CL-11 CL-K1 Collectin K1 MGC3279	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome Bloch-Sulzberger syndrome Chagas disease Klippel-Feil syndrome acquired immunodeficiency syndrome bacterial infectious disease bacterial sepsis blepharophimosis cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism disseminated intravascular coagulation enterobiasis glomerulonephritis human immunodeficiency virus infectious disease humeroradial synostosis hypertropia hypomelanosis of Ito intellectual disability intestinal schistosomiasis isolated cleft palate kidney disease learning disability mechanical strabismus nephritis nephrosis neurodegenerative disease omphalocele ophthalmoplegia pneumonia ptosis purpura fulminans pyoureter radioulnar synostosis schistosomiasis scoliosis sensorineural hearing loss spina bifida occulta spondylolisthesis strabismus trichinosis trypanosomiasis tuberculosis umbilical hernia urinary schistosomiasis viral infectious disease
81035	collectin subfamily member 12	COLEC12 CL-P1 SCARA4 SRCL	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
57393	collectrin, amino acid transport regulator	CLTRN
1435	colony stimulating factor 1	CSF1

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements