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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

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

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
91653	BOC cell adhesion associated, oncogene regulated	BOC	Homo sapiens (human)
91689	single-pass membrane protein with aspartate rich tail 1	SMDT1	Homo sapiens (human)
91694	LON peptidase N-terminal domain and ring finger 1	LONRF1	Homo sapiens (human)
91746	YTH N6-methyladenosine RNA binding protein C1	YTHDC1	Homo sapiens (human)
91748	mitotic deacetylase associated SANT domain protein	MIDEAS	Homo sapiens (human)
91754	NIMA related kinase 9	NEK9	Homo sapiens (human)
91768	Cdk5 and Abl enzyme substrate 1	CABLES1	Homo sapiens (human)
91775	neurexophilin and PC-esterase domain family member 3	NXPE3	Homo sapiens (human)
91782	charged multivesicular body protein 7	CHMP7	Homo sapiens (human)
91828	exocyst complex component 3 like 4	EXOC3L4	Homo sapiens (human)
91851	chordin like 1	CHRDL1	Homo sapiens (human)
91869	RFT1 homolog	RFT1 Aliases: CDG1N congenital disorder of glycosylation 1N	Homo sapiens (human)	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	Homo sapiens (human)
91937	T cell immunoglobulin and mucin domain containing 4	TIMD4	Homo sapiens (human)
91942	NADH:ubiquinone oxidoreductase complex assembly factor 2	NDUFAF2	Homo sapiens (human)
91949	component of oligomeric golgi complex 7	COG7	Homo sapiens (human)	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	Homo sapiens (human)
92017	sorting nexin 29	SNX29	Homo sapiens (human)
92086	gamma-glutamyltransferase light chain 1	GGTLC1	Homo sapiens (human)
92105	integrator complex subunit 4	INTS4	Homo sapiens (human)
92126	dermatan sulfate epimerase like	DSEL	Homo sapiens (human)	colorectal cancer colorectal carcinoma congenital diaphragmatic hernia diabetes mellitus hiatus hernia large intestine cancer microphthalmia type 2 diabetes mellitus
92140	metadherin	MTDH	Homo sapiens (human)
92154	MTSS I-BAR domain containing 2	MTSS2	Homo sapiens (human)
92211	cadherin related family member 1	CDHR1	Homo sapiens (human)
92241	RCSD domain containing 1	RCSD1	Homo sapiens (human)

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