GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **7926 - 7950** of **9988** in total

« First

‹ Prev

…

314

315

316

317

318

319

320

321

322

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
1585	cytochrome P450 family 11 subfamily B member 2	CYP11B2 Aliases: ALDOS CPN2 CYP11BL P-450C18 P450aldo steroid 11-beta-monooxygenase	Homo sapiens (human)	46,XY sex reversal Bartter disease Conn's syndrome IgA glomerulonephritis Liddle syndrome Waterhouse-Friderichsen syndrome abdominal obesity-metabolic syndrome 1 acromegaly acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal cortical adenoma adrenal gland cancer adrenal gland hyperfunction adrenocortical carcinoma aortic valve disease 2 aortic valve stenosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autism spectrum disorder autistic disorder brain infarction brain stem infarction cancer cardiomyopathy cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral infarction cerebrovascular disease chronic kidney disease clear cell renal cell carcinoma congenital adrenal hyperplasia congenital central hypoventilation syndrome congestive heart failure coronary artery disease coronary thrombosis corticosterone methyloxidase deficiency 1 cribriform carcinoma diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy 1H dilated cardiomyopathy disease of metabolism eclampsia embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy focal segmental glomerulosclerosis follicular adenoma glucocorticoid-remediable aldosteronism granular cell carcinoma heart disease hyperphosphatemia hyperpituitarism hypertension hypertensive heart disease hypertrophic cardiomyopathy hypokalemia kidney cancer kidney failure lactic acidosis microcystic adenoma multiple system atrophy myocardial infarction myocarditis nutmeg liver obsolete Cushing's syndrome papillary adenoma patent foramen ovale postural orthostatic tachycardia syndrome pre-eclampsia primary hyperaldosteronism prostate cancer prostate carcinoma psoriatic arthritis pulmonary edema relapsing fever renal carcinoma renal cell carcinoma renal tubular acidosis silent myocardial infarction trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus uremia
1584	cytochrome P450 family 11 subfamily B member 1	CYP11B1 Aliases: CPN1 FHI P450C11 steroid 11-beta-monooxygenase	Homo sapiens (human)	46,XY sex reversal ACTH-secreting pituitary adenoma Addison's disease Bartter disease Clouston syndrome Conn's syndrome Laron syndrome Liddle syndrome Waterhouse-Friderichsen syndrome X-linked adrenal hypoplasia congenita achondroplasia acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal cortical adenoma adrenal cortical hypofunction adrenal gland cancer adrenal gland hyperfunction adrenocortical carcinoma aromatase excess syndrome autism spectrum disorder autistic disorder autoimmune hepatitis brain infarction breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic ethmoiditis chronic sphenoidal sinusitis clear cell renal cell carcinoma congenital adrenal hyperplasia congenital central hypoventilation syndrome congestive heart failure coronary thrombosis craniosynostosis cryptorchidism disease of metabolism disorder of sexual development essential hypertension follicular adenoma glucocorticoid-remediable aldosteronism gynecomastia heart disease hepatitis hermaphroditism hypertension hypertrichosis hypertrophy of breast hypokalemia infant gynecomastia kidney cancer microcystic adenoma myocardial infarction myocarditis obsolete Cushing's syndrome osteoporosis papillary adenoma pituitary-dependent Cushing's disease placental insufficiency polycystic ovary syndrome pre-eclampsia primary hyperaldosteronism proteinuria pseudohermaphroditism renal carcinoma renal cell carcinoma renal tubular acidosis silent myocardial infarction trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
1583	cytochrome P450 family 11 subfamily A member 1	CYP11A1 Aliases: P450SCC cholesterol monooxygenase (side-chain-cleaving)	Homo sapiens (human)	3p deletion syndrome 46,XY sex reversal Addison's disease Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Angelman syndrome Bannayan-Riley-Ruvalcaba syndrome Bartter disease Cockayne syndrome Conn's syndrome Cornelia de Lange syndrome Cowden syndrome Dubowitz syndrome Fanconi anemia NFIA-related disorder Niemann-Pick disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome SATB2-associated syndrome Seckel syndrome Sertoli cell-only syndrome Silver-Russell syndrome Smith-Magenis syndrome Waterhouse-Friderichsen syndrome X-linked Aarskog syndrome X-linked adrenal hypoplasia congenita X-linked spermatogenic failure 1 adenocarcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal cortical hypofunction adrenocortical carcinoma allergic asthma asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autism spectrum disorder autistic disorder autoimmune hepatitis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome breast cancer breast carcinoma breast disease breast fibrocystic disease cancer cerebral degeneration cholera chondrodysplasia-pseudohermaphroditism syndrome choriocarcinoma chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome chronic ethmoiditis chronic sphenoidal sinusitis congenital adrenal hyperplasia congenital adrenal insufficiency cryptorchidism diabetes mellitus disorder of sexual development distal 10q deletion syndrome endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epilepsy esophagus squamous cell carcinoma essential hypertension focal epilepsy follicular adenoma gynecomastia hepatitis hepatocellular carcinoma hermaphroditism herpes zoster hyperandrogenism hyperglycemia hypertension hypertrophy of breast hypogonadism hypogonadotropic hypogonadism 23 with or without anosmia hypospadias inclusion body myositis infant gynecomastia intrinsic asthma kidney disease lactic acidosis lactocele lesion of sciatic nerve liver cancer microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microglandular adenosis nephrosis nodular prostate obesity osteoporosis ovarian hyperstimulation syndrome papillary adenoma partial motor epilepsy patent foramen ovale placenta cancer placental insufficiency polycystic ovary syndrome primary hyperaldosteronism prostate cancer prostate carcinoma prostatic adenoma pseudohermaphroditism sciatic neuropathy sphingolipidosis status epilepticus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome type 2 diabetes mellitus uterine corpus cancer visual epilepsy
1539	cylicin 2	CYLC2	Homo sapiens (human)
1538	cylicin 1	CYLC1	Homo sapiens (human)
26999	cytoplasmic FMR1 interacting protein 2	CYFIP2	Homo sapiens (human)
23191	cytoplasmic FMR1 interacting protein 1	CYFIP1	Homo sapiens (human)
1536	cytochrome b-245 beta chain	CYBB	Homo sapiens (human)
606495	cytochrome b5 reductase like	CYB5RL Aliases: LOC606495	Homo sapiens (human)
51167	cytochrome b5 reductase 4	CYB5R4 Aliases: b5+b5R dJ676J13.1	Homo sapiens (human)	breast cancer diabetes mellitus diabetic ketoacidosis gestational diabetes glucose intolerance maturity-onset diabetes of the young prediabetes syndrome type 2 diabetes mellitus
1727	cytochrome b5 reductase 3	CYB5R3 Aliases: B5R NADH-cytochrome b5 reductase 3	Homo sapiens (human)	acquired polycythemia alternating hemiplegia of childhood autonomic neuropathy bladder urothelial carcinoma brain disease breast cancer breast carcinoma cancer central nervous system disease colon cancer colonic benign neoplasm colorectal cancer contagious pustular dermatitis cowpox dystonia embryoma epilepsy erythema infectiosum erythropoietin polycythemia esotropia essential hypertension estrogen-receptor negative breast cancer exanthema subitum familial erythrocytosis 2 familial hyperlipidemia hypertension hypertropia idiopathic scoliosis intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia locked-in syndrome maple syrup urine disease mechanical strabismus methemoglobinemia microcephaly milker's nodule monocular esotropia movement disease nervous system disease ophthalmoplegia placental insufficiency polycythemia vera polycythemia quadriplegia sickle cell anemia smallpox strabismus stress polycythemia sulfhemoglobinemia syndromic X-linked intellectual disability 94 tarsal-carpal coalition syndrome thyroid adenoma thyroid cancer thyroid gland carcinoma variola major variola minor visual epilepsy
51700	cytochrome b5 reductase 2	CYB5R2	Homo sapiens (human)	cancer giant cell glioblastoma glioblastoma nasopharynx carcinoma prostate cancer prostate carcinoma
51706	cytochrome b5 reductase 1	CYB5R1 Aliases: humb5R2	Homo sapiens (human)	cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma large intestine cancer
220002	cytochrome b561 family member A3	CYB561A3	Homo sapiens (human)
347487	chromosome X open reading frame 66	CXorf66	Homo sapiens (human)
254158	chromosome X open reading frame 58	CXorf58	Homo sapiens (human)
100132994	chromosome X open reading frame 49B	CXorf49B	Homo sapiens (human)
100130361	chromosome X open reading frame 49	CXorf49	Homo sapiens (human)
51523	CXXC finger protein 5	CXXC5	Homo sapiens (human)
10663	C-X-C motif chemokine receptor 6	CXCR6	Homo sapiens (human)
643	C-X-C motif chemokine receptor 5	CXCR5	Homo sapiens (human)
7852	C-X-C motif chemokine receptor 4	CXCR4	Homo sapiens (human)
2833	C-X-C motif chemokine receptor 3	CXCR3	Homo sapiens (human)
3579	C-X-C motif chemokine receptor 2	CXCR2	Homo sapiens (human)
3577	C-X-C motif chemokine receptor 1	CXCR1	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements