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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 **8576 - 8600** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
1468	solute carrier family 25 member 10	SLC25A10	Homo sapiens (human)	mitochondrial DNA depletion syndrome 19 mitochondrial DNA depletion syndrome mitochondrial complex I deficiency myoclonic-atonic epilepsy
8402	solute carrier family 25 member 11	SLC25A11	Homo sapiens (human)	paraganglioma
8604	solute carrier family 25 member 12	SLC25A12	Homo sapiens (human)	Asperger syndrome autism spectrum disorder autistic disorder citrullinemia common bile duct disease developmental and epileptic encephalopathy 39 intrahepatic cholestasis
10165	solute carrier family 25 member 13	SLC25A13	Homo sapiens (human)	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
8034	solute carrier family 25 member 16	SLC25A16	Homo sapiens (human)
60386	solute carrier family 25 member 19	SLC25A19	Homo sapiens (human)
79085	solute carrier family 25 member 23	SLC25A23	Homo sapiens (human)
253512	solute carrier family 25 member 30	SLC25A30	Homo sapiens (human)
84275	solute carrier family 25 member 33	SLC25A33	Homo sapiens (human)
284723	solute carrier family 25 member 34	SLC25A34	Homo sapiens (human)
284427	solute carrier family 25 member 41	SLC25A41	Homo sapiens (human)
401612	solute carrier family 25 member 53	SLC25A53	Homo sapiens (human)
293	solute carrier family 25 member 6	SLC25A6	Homo sapiens (human)
10861	solute carrier family 26 member 1	SLC26A1	Homo sapiens (human)
1836	solute carrier family 26 member 2	SLC26A2 Aliases: DTDST diastrophic dysplasia sulfate transporter	Homo sapiens (human)	Baraitser-Winter syndrome Bartter disease Clostridium difficile colitis Conn's syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Pendred Syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome achondrogenesis type IB achondroplasia adenocarcinoma adenoma arthritis arthropathy atelosteogenesis auditory system disease autosomal recessive osteopetrosis 7 benign mesothelioma brachydactyly branchiootic syndrome breast cancer cancer chondrodysplasia punctata cleft palate clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure cryptorchidism cystic lymphangioma diarrhea diastrophic dysplasia disease of metabolism dyshormonogenic goiter embryoma endometritis fibrosarcoma follicular adenoma inguinal hernia irritable bowel syndrome isolated cleft palate juvenile rheumatoid arthritis large intestine cancer laryngostenosis lingual-facial-buccal dyskinesia lung benign neoplasm lung cancer lung non-small cell carcinoma malignant mesothelioma mastitis microcystic adenoma movement disease mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia 4 multiple epiphyseal dysplasia neurocirculatory asthenia omphalocele orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis osteochondrodysplasia osteopetrosis osteoporosis osteosclerosis otosclerosis papillary adenoma placental insufficiency polyhydramnios primary hyperaldosteronism scoliosis sensorineural hearing loss spinal cord disease spondylolysis stomach cancer stomach carcinoma umbilical hernia
1811	solute carrier family 26 member 3	SLC26A3	Homo sapiens (human)
375611	solute carrier family 26 member 5	SLC26A5	Homo sapiens (human)
65010	solute carrier family 26 member 6	SLC26A6	Homo sapiens (human)
115111	solute carrier family 26 member 7	SLC26A7	Homo sapiens (human)
116369	solute carrier family 26 member 8	SLC26A8	Homo sapiens (human)
115019	solute carrier family 26 member 9	SLC26A9	Homo sapiens (human)
11001	solute carrier family 27 member 2	SLC27A2	Homo sapiens (human)
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
9154	solute carrier family 28 member 1	SLC28A1	Homo sapiens (human)
9153	solute carrier family 28 member 2	SLC28A2	Homo sapiens (human)

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