Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Glycogenes Glycoproteins Lectins Glycans Pathways
Gene Symbol Gene Symbol Aliases Gene ID Disease Name ▼
  • MPS1
  • MPSI
  • mucopolysaccharidosis type I
  • Hurler syndrome
  • Hurler-Scheie syndrome
  • Scheie syndrome
GNE
  • Uae1
  • bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase
  • Hereditary inclusion body myopathy type 2
  • Nonaka myopathy
  • glucocerebrosidase
  • Gaucher disease, type I
  • Gaucher disease, type II
  • Gaucher disease, type II, neuronopathic form, classic type
  • Gaucher disease, type II, perinatal lethal form
  • Gaucher disease, type III
  • Gaucher disease, type IIIC
  • carboxypeptidase C
  • carboxypeptidase Y-like kininase
  • carboxypeptidase-L
  • deamidase
  • lysosomal carboxypeptidase A
  • lysosomal protective protein
  • urinary kininase
  • Galactosialidosis
  • GM2-AP
  • GM2-activator protein
  • GM2AP
  • SAP-3
  • cerebroside sulfate activator protein
  • sphingolipid activator protein 3
  • GM2-gangliosidosis, AB variant
  • EBP
  • elastin binding protein
  • GM1-gangliosidosis, type I
  • GM1-gangliosidosis, type II
  • GM1-gangliosidosis, type III
  • Morquio syndrome B
  • CWH41
  • DER7
  • GCS1
  • glucosidase I
  • processing A-glucosidase I
  • GCS1-CDG
  • GalNAc-T3
  • HFTC
  • HHS
  • polypeptide GalNAc transferase 3
  • GALNT3-CDG
  • a-L-fucosidase 1
  • tissue fucosidase
  • α-L-fucosidase 1
  • Fucosidosis
  • AC
  • ACDase
  • FLJ21558
  • PHP32
  • acid ceramidase
  • acylsphingosine deacylase
427
  • Farber Lipogranulomatosis
  • Farber Lipogranulomatosis, type 1
  • Farber Lipogranulomatosis, type 2
  • Farber Lipogranulomatosis, type 3
  • Farber Lipogranulomatosis, type 4
  • Farber Lipogranulomatosis, type 5
Displaying entries 51 - 60 of 1907 in total

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01