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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 **7251 - 7275** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
65258	metallophosphoesterase 1	MPPE1 Aliases: Cdc1 PGAP5 post-GPI attachment to proteins 5	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer cerebral malaria chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatitis influenza intermittent explosive disorder malaria melanoma papillary renal cell carcinoma pneumonia renal cell carcinoma sarcomatoid renal cell carcinoma skin melanoma
338675	olfactory receptor family 5 subfamily AP member 2	OR5AP2	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
11120	butyrophilin subfamily 2 member A1	BTN2A1	Homo sapiens (human)
50863	neurotrimin	NTM Aliases: CEPU-1 HNT IGLON2 IgLON family member 2 NTRI neurotrimin	Homo sapiens (human)	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
5884	RAD17 checkpoint clamp loader component	RAD17	Homo sapiens (human)
10848	protein phosphatase 1 regulatory subunit 13 like	PPP1R13L	Homo sapiens (human)
6773	signal transducer and activator of transcription 2	STAT2	Homo sapiens (human)
8863	period circadian regulator 3	PER3	Homo sapiens (human)
3508	immunoglobulin mu DNA binding protein 2	IGHMBP2	Homo sapiens (human)
9543	immunoglobulin superfamily DCC subclass member 3	IGDCC3	Homo sapiens (human)
255189	phospholipase A2 group IVF	PLA2G4F Aliases: PLA2G4F/Z	Homo sapiens (human)	arthritis arthropathy osteoarthritis
1816	dopamine receptor D5	DRD5	Homo sapiens (human)
4060	lumican	LUM	Homo sapiens (human)
388697	hornerin	HRNR	Homo sapiens (human)
10178	teneurin transmembrane protein 1	TENM1	Homo sapiens (human)
11104	katanin catalytic subunit A1	KATNA1	Homo sapiens (human)
107	adenylate cyclase 1	ADCY1	Homo sapiens (human)
25836	NIPBL cohesin loading factor	NIPBL	Homo sapiens (human)
1954	multiple EGF like domains 8	MEGF8	Homo sapiens (human)
56261	glycerophosphocholine phosphodiesterase 1	GPCPD1 Aliases: GDE5 GDPD6 KIAA1434	Homo sapiens (human)	eating disorder endometrial cancer endometrial carcinoma obesity uterine corpus cancer
828	calcyphosine	CAPS	Homo sapiens (human)
93650	acid phosphatase 4	ACP4 Aliases: testicular acid phosphatase	Homo sapiens (human)
944	TNF superfamily member 8	TNFSF8	Homo sapiens (human)
1207	chloride nucleotide-sensitive channel 1A	CLNS1A	Homo sapiens (human)

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