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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	July 8, 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 **1276 - 1300** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
32974	Zwischenferment	Zw	Drosophila melanogaster (fruit fly)	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
24377	glucose-6-phosphate dehydrogenase	G6pd	Rattus norvegicus (Norway rat)	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
51738	ghrelin and obestatin prepropeptide	GHRL	Homo sapiens (human)	Prader-Willi syndrome cardiovascular system disease diabetic neuropathy end stage renal disease esophagus adenocarcinoma middle cerebral artery infarction morbid obesity multiple endocrine neoplasia obesity obstructive sleep apnea type 2 diabetes mellitus
43436	alpha-Mannosidase class I b	alpha-Man-Ib	Drosophila melanogaster (fruit fly)	Rafiq syndrome
227619	mannosidase, alpha, class 1B, member 1	Man1b1	Mus musculus (house mouse)	Rafiq syndrome
499751	mannosidase, alpha, class 1B, member 1	Man1b1	Rattus norvegicus (Norway rat)	Rafiq syndrome
853595	mannosyl-oligosaccharide 1,2-alpha-mannosidase	MNS1	Saccharomyces cerevisiae S288C	Rafiq syndrome
8789	fructose-bisphosphatase 2	FBP2	Homo sapiens (human)	Rett syndrome X-linked ichthyosis cancer epithelioid sarcoma sarcoma spindle cell sarcoma stomach cancer stomach carcinoma
22854	netrin G1	NTNG1 Aliases: KIAA0976 Lmnt1 Netrin-G1 netrin G1f	Homo sapiens (human)	Rett syndrome anorexia nervosa autistic disorder bipolar disorder brain disease cancer cerebral infarction cerebrovascular disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma epilepsy esophagitis gastroesophageal reflux disease head and neck squamous cell carcinoma hydrocephalus intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia microcephaly morphine dependence movement disease nephrolithiasis neuroendocrine carcinoma neuroendocrine tumor neuropathy patent ductus arteriosus peptic esophagitis peripheral nervous system disease polyneuropathy schizophrenia sensorineural hearing loss uric acid nephrolithiasis visual epilepsy
3029	hydroxyacylglutathione hydrolase	HAGH Aliases: GLO2 GLXII HAGH1	Homo sapiens (human)	Rett syndrome autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease cancer carcinoma clear cell adenocarcinoma inflammatory breast carcinoma kidney failure lung cancer lung non-small cell carcinoma polycystic kidney disease 1 prostate cancer prostate carcinoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia uremia
63917	polypeptide N-acetylgalactosaminyltransferase 11	GALNT11 Aliases: GalNAc-T11 polypeptide GalNAc transferase 11	Homo sapiens (human)	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
946	sialic acid binding Ig like lectin 6	SIGLEC6 Aliases: CD327 OB-BP1 SIGLEC-6	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia colorectal cancer colorectal carcinoma large intestine cancer subacute bacterial endocarditis systemic lupus erythematosus
388512	C-type lectin domain containing 17A	CLEC17A Aliases: FLJ45910 prolectin	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia
38528	Hexosaminidase 1	Hexo1	Drosophila melanogaster (fruit fly)	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
31808	Hexosaminidase 2	Hexo2	Drosophila melanogaster (fruit fly)	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
180533	Beta-hexosaminidase A	hex-1	Caenorhabditis elegans	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
250735	fused lobes	fdl	Drosophila melanogaster (fruit fly)	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
294673	hexosaminidase subunit beta	Hexb	Rattus norvegicus (Norway rat)	Sandhoff disease lysosomal storage disease spinal muscular atrophy
15212	hexosaminidase B	Hexb	Mus musculus (house mouse)	Sandhoff disease lysosomal storage disease spinal muscular atrophy
856220	Golgi transport complex subunit COG4	COG4	Saccharomyces cerevisiae S288C	Saul-Wilson syndrome congenital disorder of glycosylation type IIj
34544	alpha-L-iduronidase	Idua	Drosophila melanogaster (fruit fly)	Scheie syndrome gastric ulcer mucopolysaccharidosis I mucopolysaccharidosis Ih/s mucopolysaccharidosis Ih otitis media
45320	terribly reduced optic lobes	trol	Drosophila melanogaster (fruit fly)	Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia carotid artery disease dextro-looped transposition of the great arteries hyperglycemia hypertension osteochondrodysplasia thanatophoric dysplasia
6716	steroid 5 alpha-reductase 2	SRD5A2 Aliases: 3-oxo-5-alpha-steroid 4-dehydrogenase 2	Homo sapiens (human)	Sertoli cell-only syndrome Turner syndrome Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 adenosarcoma alcohol dependence alcohol use disorder alopecia androgen insensitivity syndrome androgenic alopecia azoospermia breast cancer breast carcinoma cancer childhood acute lymphocytic leukemia cryptorchidism diabetes mellitus diabetic ketoacidosis disorder of sexual development embryoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis gallbladder disease gonadal dysgenesis hepatitis C hepatocellular carcinoma hermaphroditism hyperprolactinemia hypogonadotropic hypogonadism 23 with or without anosmia hypospadias liver cancer liver carcinoma liver disease nephroblastoma nodular prostate oligospermia ovarian cancer ovarian carcinoma pancreatitis peripheral artery disease phimosis polycystic ovary syndrome post-traumatic stress disorder prostate cancer prostate carcinoma prostate disease prostatic adenoma pseudohermaphroditism schizophrenia type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer
83639	testis expressed 101	TEX101 Aliases: CT131 MGC4766 SGRG SPATA44 TES101-reactive protein TES101RP cancer/testis antigen 131 spermatogenesis associated 44	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 adenocarcinoma adenoma azoospermia basal cell carcinoma breast cancer breast ductal carcinoma cancer cribriform carcinoma embryoma granular cell carcinoma hepatocellular carcinoma liver cancer oligospermia tubular adenocarcinoma
5634	phosphoribosyl pyrophosphate synthetase 2	PRPS2 Aliases: PRS II ribose-phosphate diphosphokinase 2	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 cancer embryoma oligospermia systemic lupus erythematosus

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