GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3901 - 3925** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
57175	coronin 1B	CORO1B
23603	coronin 1C	CORO1C
10391	coronin 2B	CORO2B
84940	coronin 6	CORO6
79585	coronin 7	CORO7
2017	cortactin	CTTN
83992	cortactin binding protein 2	CTTNBP2
1393	corticotropin releasing hormone binding protein	CRHBP
1394	corticotropin releasing hormone receptor 1	CRHR1
1395	corticotropin releasing hormone receptor 2	CRHR2
57585	cramped chromatin regulator homolog 1	CRAMP1
10428	craniofacial development protein 1	CFDP1
548596	creatine kinase, mitochondrial 1A	CKMT1A
1159	creatine kinase, mitochondrial 1B	CKMT1B
6997	cripto, EGF-CFC family member	CRIPTO
51340	crooked neck pre-mRNA splicing factor 1	CRNKL1
23418	crumbs cell polarity complex component 1	CRB1
286204	crumbs cell polarity complex component 2	CRB2
92359	crumbs cell polarity complex component 3	CRB3
55997	cryptic, EGF-CFC family member 1	CFC1 CRYPTIC	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 B-cell lymphoma Langerhans-cell histiocytosis Marfan syndrome Pick's disease Reye syndrome aromatase excess syndrome arteriosclerotic cardiovascular disease atherosclerosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrioventricular septal defect autoimmune hepatitis biliary atresia cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiovascular system disease cerebral degeneration congenital adrenal hyperplasia congenital heart disease coronary artery disease dextro-looped transposition of the great arteries disease of metabolism double outlet right ventricle embryoma essential thrombocythemia gallbladder disease gastric adenocarcinoma gastrointestinal system cancer heart disease hepatitis liver disease lymphoma malaria multiple types of congenital heart defects 6 myelodysplastic syndrome neuroblastoma non-Hodgkin lymphoma obsolete dextro-looped transposition of the great arteries 1 obsolete ymphosarcoma patent foramen ovale reticulosarcoma right atrial isomerism schizophrenia situs inversus tuberculosis tuberous sclerosis visceral heterotaxy
653275	cryptic, EGF-CFC family member 1B	CFC1B
1407	cryptochrome circadian regulator 1	CRY1	delayed sleep phase syndrome
1409	crystallin alpha A	CRYAA
102724652	crystallin alpha A2	LOC102724652
1410	crystallin alpha B	CRYAB

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