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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 **6226 - 6250** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
3161	hyaluronan mediated motility receptor	HMMR Aliases: CD168 RHAMM	Homo sapiens (human)	Crohn's colitis Crohn's disease Ewing sarcoma Richter's syndrome acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult lymphoma agranulocytosis anaplastic astrocytoma arthritis arthropathy atrophy of testis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome bladder carcinoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral primitive neuroectodermal tumor cervical adenocarcinoma cervical cancer cervix carcinoma childhood cerebral astrocytoma childhood leukemia childhood lymphoma choriocarcinoma chromophobe renal cell carcinoma chromosome 5q deletion syndrome chronic leukemia chronic lymphocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma diffuse large B-cell lymphoma embryoma endometrial cancer endometrial carcinoma epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor fibrillary astrocytoma gemistocytic astrocytoma gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma hepatitis B hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease invasive ductal carcinoma juvenile pilocytic astrocytoma large intestine cancer leiomyosarcoma leukemia leukopenia liver cancer luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung disease lung non-small cell carcinoma lymphoblastic lymphoma lymphoma lymphoplasmacytic lymphoma macroglobulinemia malignant astrocytoma malignant peripheral nerve sheath tumor medulloblastoma medulloepithelioma microphthalmia mixed glioma multiple myeloma myxoid leiomyosarcoma neurilemmoma neuroectodermal tumor neurofibrosarcoma neutropenia nodular prostate nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma ossifying fibroma osteoarthritis ovarian cancer ovarian carcinoma oxyphilic adenoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma pilocytic astrocytoma placenta cancer polycystic ovary syndrome prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma renal carcinoma renal cell carcinoma renal oncocytoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma seminoma severe congenital neutropenia sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma supratentorial primitive neuroectodermal tumor testicular cancer testicular germ cell cancer testis seminoma tongue squamous cell carcinoma transitional cell carcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer
22993	HMG-box containing 3	HMGXB3	Homo sapiens (human)
79366	high mobility group nucleosome binding domain 5	HMGN5	Homo sapiens (human)
3158	3-hydroxy-3-methylglutaryl-CoA synthase 2	HMGCS2	Homo sapiens (human)	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 HMG-CoA synthase 2 deficiency Pick's disease Reye syndrome Riley-Day syndrome breast cancer breast carcinoma cancer carcinoma cerebral degeneration colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease diabetes mellitus diabetic ketoacidosis diarrhea embryoma epilepsy esophagus squamous cell carcinoma essential hypertension extrahepatic cholestasis gallbladder disease hepatitis C hepatocellular carcinoma hypertension hypoglycemia impotence large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease obsolete type 1 diabetes mellitus 9 ovarian carcinoma premature ejaculation prostate cancer prostate carcinoma psychologic dyspareunia rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus visual epilepsy
3157	3-hydroxy-3-methylglutaryl-CoA synthase 1	HMGCS1 Aliases: 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase	Homo sapiens (human)	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatitis C hepatoblastoma hepatocellular carcinoma large intestine cancer obesity prostate cancer prostate carcinoma spinal cord disease
3156	3-hydroxy-3-methylglutaryl-CoA reductase	HMGCR	Homo sapiens (human)
54511	3-hydroxy-3-methylglutaryl-CoA lyase like 1	HMGCLL1 Aliases: DKFZP434G1411 bA418P12.1	Homo sapiens (human)	chronic myeloid leukemia
3155	3-hydroxy-3-methylglutaryl-CoA lyase	HMGCL Aliases: HL hydroxymethylglutaricaciduria hydroxymethylglutaryl-CoA lyase	Homo sapiens (human)	Unverricht-Lundborg syndrome X-linked dilated cardiomyopathy acute pancreatitis amino acid metabolic disorder anemia blepharospasm brain disease cancer cardiac arrest congestive heart failure diarrhea dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy early myoclonic encephalopathy epilepsy focal hand dystonia hyperlysinemia hyperuricemia hypoglycemia hypoglycemic coma intellectual disability lactic acidosis learning disability leukopenia macrocytic anemia melanoma microcephaly mitochondrial metabolism disease mitochondrial myopathy obsolete infantile epileptic encephalopathy pancreatitis skin melanoma syndromic X-linked intellectual disability 94 thrombocytosis urea cycle disorder visual epilepsy
3146	high mobility group box 1	HMGB1	Homo sapiens (human)
256158	hemicentin 2	HMCN2	Homo sapiens (human)
83872	hemicentin 1	HMCN1	Homo sapiens (human)
56941	5-hydroxymethylcytosine binding, ES cell specific	HMCES	Homo sapiens (human)
81502	histocompatibility minor 13	HM13	Homo sapiens (human)
3135	major histocompatibility complex, class I, G	HLA-G	Homo sapiens (human)
3134	major histocompatibility complex, class I, F	HLA-F	Homo sapiens (human)
3133	major histocompatibility complex, class I, E	HLA-E	Homo sapiens (human)
3127	major histocompatibility complex, class II, DR beta 5	HLA-DRB5	Homo sapiens (human)
3126	major histocompatibility complex, class II, DR beta 4	HLA-DRB4	Homo sapiens (human)
3125	major histocompatibility complex, class II, DR beta 3	HLA-DRB3	Homo sapiens (human)
3123	major histocompatibility complex, class II, DR beta 1	HLA-DRB1	Homo sapiens (human)
3122	major histocompatibility complex, class II, DR alpha	HLA-DRA	Homo sapiens (human)
3120	major histocompatibility complex, class II, DQ beta 2	HLA-DQB2	Homo sapiens (human)
3119	major histocompatibility complex, class II, DQ beta 1	HLA-DQB1	Homo sapiens (human)
3118	major histocompatibility complex, class II, DQ alpha 2	HLA-DQA2	Homo sapiens (human)
3117	major histocompatibility complex, class II, DQ alpha 1	HLA-DQA1	Homo sapiens (human)

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