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 **301 - 325** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
15452	hypoxanthine phosphoribosyltransferase 1	Hprt1	HRPT-related hyperuricemia Lesch-Nyhan syndrome hepatocellular carcinoma
18294	8-oxoguanine DNA-glycosylase 1	Ogg1	Graves' disease Parkinson's disease angiomyolipoma basal cell carcinoma breast cancer cataract cholangiocarcinoma coronary artery disease gestational diabetes head and neck squamous cell carcinoma hepatitis hypertension middle cerebral artery infarction ovarian cancer pancreatic cancer pre-eclampsia primary open angle glaucoma progressive supranuclear palsy prostate cancer pterygium renal cell carcinoma senile cataract status epilepticus transient cerebral ischemia transitional cell carcinoma type 2 diabetes mellitus
14466	glucosylceramidase beta 1	Gba1	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Netherton syndrome Parkinson's disease Parkinsonism late onset Parkinson's disease psoriasis
50798	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Gne	GNE myopathy sialuria
14667	GM2 ganglioside activator protein	Gm2a	GM2 gangliosidosis, AB variant GM2 gangliosidosis
12091	galactosidase, beta 1	Glb1	GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis mucopolysaccharidosis IV mucopolysaccharidosis type IVB
246179	fukutin	Fktn	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
17939	N-acetyl galactosaminidase, alpha	Naga	Fabry disease Kanzaki disease Schindler disease type 1 angiokeratoma neuroaxonal dystrophy
117592	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	B3galt6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
218271	beta-1,4-galactosyltransferase 7	B4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
72136	carbohydrate sulfotransferase 14	Chst14	Ehlers-Danlos syndrome musculocontractural type 1
80294	protein O-fucosyltransferase 2	Pofut2	Down syndrome
140484	protein O-fucosyltransferase 1	Pofut1	Dowling-Degos disease
224143	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
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
233781	xylosyltransferase 1	Xylt1	Desbuquois dysplasia kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
235582	glycerate kinase	Glyctk	D-glyceric aciduria
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
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
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
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
14420	galactosylceramidase	Galc	Creutzfeldt-Jakob disease Krabbe disease Mycoplasma pneumoniae pneumonia melanoma
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
72145	WD repeat and FYVE domain containing 3	Wdfy3	Chediak-Higashi syndrome autism spectrum disorder primary autosomal dominant microcephaly 18
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

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