GlyCosmos Portal

Mus musculus (house mouse)

Summary

Taxonomy ID: 10090
PubChem Taxonomy: 10090

Genes (662) Glycans (1270) Glycoproteins (13000) Lectins (276) Pathways (1335)

Displaying entries **26 - 50** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
14447	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	Gapdhs	Alzheimer's disease
22059	transformation related protein 53	Trp53	B-lymphoblastic leukemia/lymphoma CHARGE syndrome Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome T-cell non-Hodgkin lymphoma acute myeloid leukemia adenoid cystic carcinoma aggressive NK-cell leukemia angiosarcoma basal cell carcinoma breast cancer bronchiolo-alveolar adenocarcinoma bronchopulmonary dysplasia cancer cervical adenocarcinoma cervical squamous cell carcinoma cholesteatoma of middle ear choroid plexus papilloma clear cell renal cell carcinoma colorectal adenocarcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis diffuse large B-cell lymphoma dilated cardiomyopathy disease of cellular proliferation ductal carcinoma in situ dyskeratosis congenita endometrial adenocarcinoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma glioblastoma graft-versus-host disease hematologic cancer hepatocellular carcinoma high grade glioma ischemia leukemia low tension glaucoma lung non-small cell carcinoma malignant peripheral nerve sheath tumor medulloblastoma melanoma meninges sarcoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome myelofibrosis nasal cavity cancer nasopharynx carcinoma oral mucosa leukoplakia oral squamous cell carcinoma oral submucous fibrosis osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paranasal sinus benign neoplasm pre-malignant neoplasm primary open angle glaucoma prostate cancer pterygium renal cell carcinoma sarcoma serous cystadenocarcinoma squamous cell carcinoma stomach cancer testicular cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma traumatic brain injury urinary bladder cancer vascular dementia
56297	ADP-ribosylation factor-like 6	Arl6	Bardet-Biedl syndrome 1 Bardet-Biedl syndrome 3 Bardet-Biedl syndrome ciliopathy retinitis pigmentosa 55
280645	beta-1,3-glucuronyltransferase 2	B3gat2	Barrett's esophagus schizophrenia
16535	potassium voltage-gated channel, subfamily Q, member 1	Kcnq1	Beckwith-Wiedemann syndrome Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation heart conduction disease hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
24088	toll-like receptor 2	Tlr2	Behcet's disease Kuhnt-Junius degeneration acne acute necrotizing pancreatitis allergic rhinitis alveolar echinococcosis anogenital venereal wart anterior uveitis asthma atopic dermatitis atrial fibrillation bacterial pneumonia breast cancer carotid stenosis cholesteatoma of middle ear cholesteatoma collagen disease colorectal cancer cutaneous leishmaniasis cystic echinococcosis dermatomyositis diffuse scleroderma dry eye syndrome end stage renal disease eye disease gastroesophageal reflux disease glucose metabolism disease hepatocellular carcinoma ileitis keratitis keratoconjunctivitis kidney failure leprosy lung disease mastoiditis meningococcal meningitis molluscum contagiosum otitis media pancreatitis perinatal necrotizing enterocolitis primary immunodeficiency disease prostate cancer psoriasis pulmonary sarcoidosis pulmonary tuberculosis renal fibrosis rhinitis seborrheic dermatitis severe acute respiratory syndrome sinusitis skin papilloma suppurative otitis media tuberculosis type 1 diabetes mellitus urinary bladder cancer urinary tract infection vitiligo
12833	collagen, type VI, alpha 1	Col6a1	Bethlem myopathy Ullrich congenital muscular dystrophy congenital muscular dystrophy muscular dystrophy
333433	glycerol-3-phosphate dehydrogenase 1-like	Gpd1l	Brugada syndrome 2
17869	myelocytomatosis oncogene	Myc	Burkitt lymphoma acute lymphoblastic leukemia acute promyelocytic leukemia angiosarcoma breast cancer cancer chronic lymphocytic leukemia clear cell renal cell carcinoma coronary restenosis demyelinating disease hepatitis C hepatocellular carcinoma hyperparathyroidism leiomyoma liver cirrhosis lung adenocarcinoma lung cancer nephroblastoma obesity osteoporosis polycystic kidney disease 1 polycystic kidney disease prolactinoma prostate adenocarcinoma prostate cancer prostatic hypertrophy pulmonary hypertension renal cell carcinoma rhabdoid cancer thyroid gland papillary carcinoma urinary bladder cancer
18706	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	Pik3ca	CLOVES syndrome Cowden syndrome 5 autosomal recessive polycystic kidney disease breast angiosarcoma breast cancer cerebral cavernous malformation colon adenocarcinoma colorectal cancer colorectal carcinoma cutaneous Paget's disease epidermal nevus esophageal cancer estrogen-receptor positive breast cancer hepatocellular carcinoma lung cancer ovarian cancer rectal benign neoplasm seborrheic keratosis stomach cancer
80908	ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase	Abo	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
16177	interleukin 1 receptor, type I	Il1r1	COVID-19 cholesteatoma of middle ear chronic recurrent multifocal osteomyelitis pulpitis severe acute respiratory syndrome systemic scleroderma type 1 diabetes mellitus
21419	transcription factor AP-2 beta	Tfap2b	Char syndrome angle-closure glaucoma patent ductus arteriosus sleep disorder
15275	hexokinase 1	Hk1	Charcot-Marie-Tooth disease type 4G acute lymphoblastic leukemia anemia colorectal cancer congenital nonspherocytic hemolytic anemia glucose metabolism disease multiple myeloma obesity pulmonary hypertension retinitis pigmentosa sickle cell anemia urinary bladder cancer
72145	WD repeat and FYVE domain containing 3	Wdfy3	Chediak-Higashi syndrome autism spectrum disorder primary autosomal dominant microcephaly 18
11651	thymoma viral proto-oncogene 1	Akt1	Cowden syndrome 6 Parkinson's disease Proteus syndrome alcohol use disorder autosomal recessive polycystic kidney disease bipolar disorder brain ischemia breast cancer cancer chronic myeloid leukemia colon cancer colorectal cancer diabetic retinopathy esophageal cancer esophagus squamous cell carcinoma hepatocellular carcinoma hypertension idiopathic pulmonary fibrosis impotence in situ carcinoma intermediate coronary syndrome invasive ductal carcinoma lung non-small cell carcinoma malignant astrocytoma myocardial infarction ovarian cancer pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paraplegia prostate adenocarcinoma prostate cancer pulmonary tuberculosis renal cell carcinoma schizophrenia type 2 diabetes mellitus ureteral obstruction urinary bladder cancer vulva cancer
14420	galactosylceramidase	Galc	Creutzfeldt-Jakob disease Krabbe disease Mycoplasma pneumoniae pneumonia melanoma
394436	UDP glucuronosyltransferase 1 family, polypeptide A1	Ugt1a1	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome bilirubin metabolic disorder breast cancer cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer type 1 diabetes mellitus type 2 diabetes mellitus
18654	placental growth factor	Pgf	Crohn's disease amyotrophic lateral sclerosis ankylosing spondylitis asthma brain ischemia breast cancer carotid artery disease congestive heart failure diabetic neuropathy diabetic retinopathy end stage renal disease epilepsy glioblastoma hypertension limited scleroderma liver cirrhosis lymphedema myocardial infarction obesity pancreatic endocrine carcinoma pre-eclampsia pulmonary hypertension pyelonephritis renal cell carcinoma rheumatoid arthritis sickle cell anemia status epilepticus systemic lupus erythematosus temporal lobe epilepsy
269951	isocitrate dehydrogenase 2 (NADP+), mitochondrial	Idh2	D-2-hydroxyglutaric aciduria 2 acute myeloid leukemia bone remodeling disease esophagus squamous cell carcinoma hepatocellular carcinoma hepatocellular clear cell carcinoma high grade glioma intrahepatic cholangiocarcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma lung squamous cell carcinoma status epilepticus stomach cancer
15926	isocitrate dehydrogenase 1 (NADP+), soluble	Idh1	D-2-hydroxyglutaric aciduria acute myeloid leukemia autoimmune disease cancer glioblastoma hepatocellular clear cell carcinoma high grade glioma lung adenocarcinoma lung squamous cell carcinoma myelodysplastic syndrome
235582	glycerate kinase	Glyctk	D-glyceric aciduria
233781	xylosyltransferase 1	Xylt1	Desbuquois dysplasia kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
15531	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Ndst1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
224143	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy

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