GlyCosmos Portal

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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 **9026 - 9050** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
55243	kirre like nephrin family adhesion molecule 1	KIRREL1	Homo sapiens (human)
348174	C-type lectin domain family 18 member A	CLEC18A	Homo sapiens (human)
5228	placental growth factor	PGF	Homo sapiens (human)
7532	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma	YWHAG	Homo sapiens (human)
6527	solute carrier family 5 member 4	SLC5A4	Homo sapiens (human)
9466	interleukin 27 receptor subunit alpha	IL27RA	Homo sapiens (human)
26530	olfactory receptor family 12 subfamily D member 1 (gene/pseudogene)	OR12D1	Homo sapiens (human)
349667	reticulon 4 receptor like 2	RTN4RL2 Aliases: NGRH1 NgR2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
10998	solute carrier family 27 member 5	SLC27A5 Aliases: ACSB ACSVL6 FACVL3 FATP5 FLJ22987 VLACSR VLCS-H2 VLCSH2 fatty-acid-Coenzyme A ligase, very long-chain 3	Homo sapiens (human)	B-cell lymphoma Bloch-Sulzberger syndrome Goodpasture syndrome Loeffler syndrome Takayasu's arteritis X-linked chronic granulomatous disease abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome agranulocytosis allergic asthma asthma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease brain disease bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic granulomatous disease chronic obstructive pulmonary disease complement deficiency cutaneous porphyria cystic fibrosis embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria esophagus squamous cell carcinoma extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis farmer's lung gastric lymphoma giardiasis granulomatosis with polyangiitis hepatitis hepatocellular carcinoma hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza interstitial lung disease intrinsic asthma leukopenia liver cancer liver cirrhosis lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 neutropenia newborn respiratory distress syndrome obesity obsolete ymphosarcoma pneumocystosis pneumonia polyarteritis nodosa postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia psychotic disorder pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis red-green color blindness sarcoidosis sarcoma schizoaffective disorder schizophrenia schizophreniform disorder scleroderma severe congenital neutropenia spindle cell sarcoma steatotic liver disease systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma tuberculosis tuberculous pneumothorax uveoparotid fever
643414	lipase family member K	LIPK Aliases: bA186O14.2	Homo sapiens (human)
133482	solute carrier organic anion transporter family member 6A1	SLCO6A1	Homo sapiens (human)
150483	tektin 4	TEKT4	Homo sapiens (human)
5775	protein tyrosine phosphatase non-receptor type 4	PTPN4	Homo sapiens (human)
84804	major facilitator superfamily domain containing 9	MFSD9	Homo sapiens (human)
8323	frizzled class receptor 6	FZD6	Homo sapiens (human)
54963	uridine-cytidine kinase 1 like 1	UCKL1	Homo sapiens (human)
29888	striatin 4	STRN4	Homo sapiens (human)
56134	protocadherin alpha subfamily C, 2	PCDHAC2	Homo sapiens (human)
27345	potassium calcium-activated channel subfamily M regulatory beta subunit 4	KCNMB4	Homo sapiens (human)
56953	5',3'-nucleotidase, mitochondrial	NT5M Aliases: dNT-2 dNT2 mdN	Homo sapiens (human)	Miller-Dieker lissencephaly syndrome Smith-Magenis syndrome
11072	dual specificity phosphatase 14	DUSP14	Homo sapiens (human)
84932	RAB2B, member RAS oncogene family	RAB2B Aliases: FLJ14824	Homo sapiens (human)
390036	olfactory receptor family 52 subfamily K member 1	OR52K1	Homo sapiens (human)
10237	solute carrier family 35 member B1	SLC35B1 Aliases: ATP/ADP exchanger in the ER membrane AXER UGTREL1	Homo sapiens (human)
84735	carnosine dipeptidase 1	CNDP1	Homo sapiens (human)

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