GlyCosmos Portal

Mus musculus (house mouse)

Summary

Taxonomy ID: 10090
PubChem Taxonomy: 10090

Genes (6551) Glycans (1270) Glycoproteins (10558) Lectins (248) Pathways (1301)

Displaying entries **51 - 75** of **6551** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
12774	C-C motif chemokine receptor 5	Ccr5	Coronavirus infectious disease
140474	mucin 4	Muc4	Coronavirus infectious disease
76142	protein phosphatase 1, regulatory inhibitor subunit 14C	Ppp1r14c	Coronavirus infectious disease
19122	prion protein	Prnp	Creutzfeldt-Jakob disease Gerstmann-Straussler-Scheinker syndrome fatal familial insomnia
15488	hydroxysteroid (17-beta) dehydrogenase 4	Hsd17b4	D-bifunctional protein deficiency
16784	lysosomal-associated membrane protein 2	Lamp2	Danon disease
12728	chloride channel, voltage-sensitive 5	Clcn5	Dent disease
76025	calcium activated nucleotidase 1	Cant1	Desbuquois dysplasia
21813	transforming growth factor, beta receptor II	Tgfbr2	DiGeorge syndrome Loeys-Dietz syndrome cleft soft palate prostate cancer
22339	vascular endothelial growth factor A	Vegfa	DiGeorge syndrome amyotrophic lateral sclerosis type 1 newborn respiratory distress syndrome psoriasis
15531	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Ndst1	DiGeorge syndrome congenital diaphragmatic hernia newborn respiratory distress syndrome
14179	fibroblast growth factor 8	Fgf8	DiGeorge syndrome tetralogy of Fallot
12929	v-crk avian sarcoma virus CT10 oncogene homolog-like	Crkl	DiGeorge syndrome velocardiofacial syndrome
12667	chordin	Chrd	DiGeorge syndrome velocardiofacial syndrome
67784	plexin D1	Plxnd1	DiGeorge syndrome
226844	feline leukemia virus subgroup C cellular receptor 1	Flvcr1	Diamond-Blackfan anemia
14725	low density lipoprotein receptor-related protein 2	Lrp2	Donnai-Barrow syndrome Fanconi syndrome degenerative myopia
216616	epidermal growth factor-containing fibulin-like extracellular matrix protein 1	Efemp1	Doyne honeycomb retinal dystrophy
20265	sodium channel, voltage-gated, type I, alpha	Scn1a	Dravet syndrome autism spectrum disorder generalized epilepsy with febrile seizures plus
99377	spalt like transcription factor 4	Sall4	Duane-radial ray syndrome otitis media
13040	cathepsin S	Ctss	Duchenne muscular dystrophy
12166	bone morphogenetic protein receptor, type 1A	Bmpr1a	Ebstein anomaly Wolff-Parkinson-White syndrome chromosome 10q23 deletion syndrome juvenile polyposis syndrome osteoarthritis
12831	collagen, type V, alpha 1	Col5a1	Ehlers-Danlos syndrome classic type 1
17022	lumican	Lum	Ehlers-Danlos syndrome classic type 1
12832	collagen, type V, alpha 2	Col5a2	Ehlers-Danlos syndrome classic type 1