GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **8001 - 8025** of **9988** in total

« First

‹ Prev

…

317

318

319

320

321

322

323

324

325

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
91653	BOC cell adhesion associated, oncogene regulated	BOC
91689	single-pass membrane protein with aspartate rich tail 1	SMDT1
91694	LON peptidase N-terminal domain and ring finger 1	LONRF1
91746	YTH N6-methyladenosine RNA binding protein C1	YTHDC1
91748	mitotic deacetylase associated SANT domain protein	MIDEAS
91754	NIMA related kinase 9	NEK9
91768	Cdk5 and Abl enzyme substrate 1	CABLES1
91775	neurexophilin and PC-esterase domain family member 3	NXPE3
91782	charged multivesicular body protein 7	CHMP7
91828	exocyst complex component 3 like 4	EXOC3L4
91851	chordin like 1	CHRDL1
91869	RFT1 homolog	RFT1 CDG1N congenital disorder of glycosylation 1N	Crohn's colitis Crohn's disease Laron syndrome Unverricht-Lundborg syndrome West syndrome achondroplasia blepharospasm blindness blood coagulation disease cancer clubfoot congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis early myoclonic encephalopathy epilepsy focal hand dystonia hypertropia inflammatory bowel disease 1 inflammatory bowel disease mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy obsolete inherited blood coagulation disease ophthalmoplegia schizophrenia sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 type 2 diabetes mellitus ulcerative colitis visual epilepsy
91875	tetratricopeptide repeat domain 5	TTC5
91937	T cell immunoglobulin and mucin domain containing 4	TIMD4
91942	NADH:ubiquinone oxidoreductase complex assembly factor 2	NDUFAF2
91949	component of oligomeric golgi complex 7	COG7	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease genetic disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss
91978	tubulin polyglutamylase complex subunit 1	TPGS1
92017	sorting nexin 29	SNX29
92086	gamma-glutamyltransferase light chain 1	GGTLC1
92105	integrator complex subunit 4	INTS4
92126	dermatan sulfate epimerase like	DSEL	colorectal cancer colorectal carcinoma congenital diaphragmatic hernia diabetes mellitus hiatus hernia large intestine cancer microphthalmia type 2 diabetes mellitus
92140	metadherin	MTDH
92154	MTSS I-BAR domain containing 2	MTSS2
92211	cadherin related family member 1	CDHR1
92241	RCSD domain containing 1	RCSD1

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