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 **6251 - 6275** of **9988** in total

« First

‹ Prev

…

247

248

249

250

251

252

253

254

255

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
3115	major histocompatibility complex, class II, DP beta 1	HLA-DPB1	Homo sapiens (human)
3113	major histocompatibility complex, class II, DP alpha 1	HLA-DPA1	Homo sapiens (human)
3112	major histocompatibility complex, class II, DO beta	HLA-DOB	Homo sapiens (human)
3111	major histocompatibility complex, class II, DO alpha	HLA-DOA	Homo sapiens (human)
3109	major histocompatibility complex, class II, DM beta	HLA-DMB	Homo sapiens (human)
3108	major histocompatibility complex, class II, DM alpha	HLA-DMA	Homo sapiens (human)
3107	major histocompatibility complex, class I, C	HLA-C	Homo sapiens (human)
3106	major histocompatibility complex, class I, B	HLA-B	Homo sapiens (human)
3105	major histocompatibility complex, class I, A	HLA-A	Homo sapiens (human)
80201	hexokinase domain containing 1	HKDC1 Aliases: FLJ22761 FLJ37767	Homo sapiens (human)	breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer colorectal cancer colorectal carcinoma cone-rod dystrophy corneal disease embryoma fundus albipunctatus gestational diabetes glucose metabolism disease hepatitis hyperglycemia hyperinsulinemic hypoglycemia keratoconus large intestine cancer late-onset retinal degeneration lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young retinitis pigmentosa steatotic liver disease
3101	hexokinase 3	HK3	Homo sapiens (human)	acute promyelocytic leukemia breast cancer cancer colorectal cancer colorectal carcinoma gallbladder disease glucose metabolism disease hyperglycemia hyperinsulinemic hypoglycemia large intestine cancer liver disease maturity-onset diabetes of the young myofibroma uterine fibroid
3099	hexokinase 2	HK2	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zollinger-Ellison syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction adult medulloblastoma alcoholic hepatitis alcoholic liver cirrhosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease arthritis arthropathy autosomal recessive distal hereditary motor neuronopathy 1 bile duct adenocarcinoma bile duct cancer bile duct carcinoma bone osteosarcoma brain cancer breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest central nervous system cancer central nervous system lymphoma cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cryptococcosis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma distal arthrogryposis early infantile epileptic encephalopathy embryoma endometrial adenocarcinoma epithelioid sarcoma esophagus squamous cell carcinoma extrahepatic bile duct carcinoma fundus albipunctatus gallbladder cancer gallbladder carcinoma gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance glucose metabolism disease head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intrahepatic cholangiocarcinoma inverted follicular keratosis keratoacanthoma large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer lateral sclerosis leukemia liver cancer liver carcinoma liver cirrhosis low tension glaucoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lymphoma maturity-onset diabetes of the young medulloblastoma medullomyoblastoma melanoacanthoma melanotic medulloblastoma microphthalmia middle cerebral artery infarction mixed glioma motor neuron disease multiple myeloma myocardial infarction neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete Opitz-GBBB syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma prediabetes syndrome primary open angle glaucoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinitis pigmentosa rheumatoid arthritis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis silent myocardial infarction skin disease spindle cell sarcoma squamous cell carcinoma stomach cancer stomach carcinoma thyroid gland anaplastic carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell 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 type 2 diabetes mellitus uveal melanoma viral infectious disease
3098	hexokinase 1	HK1	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 Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Gilbert syndrome Gilles de la Tourette syndrome Klatskin's tumor Lyme disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome acute lymphoblastic leukemia adult acute lymphocytic leukemia adult fibrosarcoma agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood amyotrophic lateral sclerosis anemia arthritis arthropathy attention deficit hyperactivity disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autonomic neuropathy biliary papillomatosis bilirubin metabolic disorder bladder carcinoma blindness brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system disease cerebral degeneration childhood acute lymphocytic leukemia childhood leukemia cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis chronic lymphocytic leukemia colorectal cancer colorectal carcinoma cone-rod dystrophy congenital hemolytic anemia congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital nonspherocytic hemolytic anemia congenital stationary night blindness 1A congenital stationary night blindness coronary artery disease cystinuria diabetes mellitus diabetic ketoacidosis diabetic macular edema embryoma endometriosis of uterus endometriosis epilepsy favism fibrosarcoma fundus albipunctatus galactosemia giant cell glioblastoma glioblastoma gliosarcoma glucose metabolism disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemoglobinopathy hemolytic anemia hepatoblastoma hepatocellular carcinoma hereditary elliptocytosis hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spherocytosis high grade glioma hypoglycemia immune system disease inclusion body myositis insulinoma intellectual disability intestinal volvulus large intestine cancer learning disability leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia malaria maturity-onset diabetes of the young megaconial type congenital muscular dystrophy melanoma microphthalmia mixed glioma motor peripheral neuropathy multiple myeloma muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myelomeningocele nemaline myopathy neonatal jaundice nervous system disease neurodegenerative disease neurogenic arthropathy neuropathy night blindness normocytic anemia obesity obsolete Matthew-Wood syndrome obsolete asthenopia obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete hilar cholangiocellular carcinoma obsolete type 1 diabetes mellitus 9 osteoarthritis pancreatic ductal adenocarcinoma parasitic protozoa infectious disease peripheral nervous system disease placental insufficiency primary biliary cholangitis primary pulmonary hypertension progressive muscular atrophy pulmonary hypertension pyruvate kinase deficiency of red cells retinitis pigmentosa rheumatoid arthritis rigid spine muscular dystrophy 1 schizophrenia sickle cell anemia skin melanoma speech disorder spina bifida squamous cell carcinoma stomach cancer stomach carcinoma tethered spinal cord syndrome thalassemia tongue squamous cell 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 type 2 diabetes mellitus urinary bladder cancer
148738	hemojuvelin BMP co-receptor	HJV Aliases: HFE2A JH RGMC haemojuvelin hemojuvelin repulsive guidance molecule c	Homo sapiens (human)	Duchenne muscular dystrophy Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kallmann syndrome Meckel syndrome 8 Sheehan syndrome Wilson disease X-linked dilated cardiomyopathy amenorrhea anaplastic astrocytoma androgen insensitivity syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autosomal recessive polycystic kidney disease azoospermia bacterial infectious disease beta thalassemia breast cancer breast carcinoma cardiomyopathy cerebral infarction cerebrovascular disease childhood cerebral astrocytoma cholestasis chronic kidney disease congenital hypothyroidism congenital nongoitrous hypothyroidism 4 congestive heart failure coronary artery disease diabetes mellitus diabetic ketoacidosis 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 endomyocardial fibrosis essential hypertension essential thrombocythemia fibrillary astrocytoma gemistocytic astrocytoma hemochromatosis type 1 hemochromatosis type 2 hemochromatosis type 2A hemochromatosis hepatitis C hepatocellular carcinoma high grade glioma hypertension hypertrophic cardiomyopathy hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism impotence infertility iron metabolism disease isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma kwashiorkor liver cancer lung squamous cell carcinoma malignant astrocytoma marasmus microcytic anemia middle cerebral artery infarction muscular dystrophy myelodysplastic syndrome myxedema neurogenic arthropathy nutrition disease obesity osteoporosis panhypopituitarism pilocytic astrocytoma polycystic kidney disease 4 porphyria cutanea tarda premature ejaculation protein-energy malnutrition protoplasmic astrocytoma psychologic dyspareunia sick sinus syndrome steatotic liver disease subependymal giant cell astrocytoma thalassemia
55355	Holliday junction recognition protein	HJURP	Homo sapiens (human)
59269	HIVEP zinc finger 3	HIVEP3	Homo sapiens (human)
3097	HIVEP zinc finger 2	HIVEP2	Homo sapiens (human)
3096	HIVEP zinc finger 1	HIVEP1	Homo sapiens (human)
8479	HIRA interacting protein 3	HIRIP3	Homo sapiens (human)
7290	histone cell cycle regulator	HIRA	Homo sapiens (human)
10114	homeodomain interacting protein kinase 3	HIPK3	Homo sapiens (human)
28996	homeodomain interacting protein kinase 2	HIPK2	Homo sapiens (human)
204851	homeodomain interacting protein kinase 1	HIPK1	Homo sapiens (human)
9026	huntingtin interacting protein 1 related	HIP1R	Homo sapiens (human)
3092	huntingtin interacting protein 1	HIP1	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