chondroitin sulfate N-acetylgalactosaminyltransferase 1

Summary
Gene Symbol
  • CSGALNACT1
Aliases
  • CSGalNAcT-1
  • ChGn
  • FLJ11264
  • chondroitin beta1,4 N-acetylgalactosaminyltransferase
  • glucuronylgalactosylproteoglycan 4-beta-N- acetylgalactosaminyltransferase
Organism
Homo sapiens (human)
External Links
NCBI Gene
55790
GGDB ID
HGNC
24290
mRNA
map
  • 8p21.3
Protein
OMIM
KEGG Gene ID
hsa:55790
PubChem
55790
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Coiled coil
  • Disease variant
  • Dwarfism
  • Glycoprotein
  • Golgi apparatus
  • Metal-binding
  • Reference proteome
  • Signal-anchor
  • Transferase
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q8TDX6
  • Chondroitin beta-1,4-N-acetylgalactosaminyltransferase 1
Gene Ontology (GO)
GO Hierarchy
GlycoGene Database (GGDB)
GGDB ID
gg165
Gene Symbol
  • CSGALNACT1
Reactions
Displaying all 5 entries
Donor Acceptor Product Reference
UDP-GalNAc
G14371GV
G40609EP
UDP-GalNAc
G40723NG
G97081WO
UDP-GalNAc
G76533UX
G70907ST
UDP-GalNAc
G33235EO
UDP-GalNAc
G48258CR
G07747BZ
Orthologous Gene
KEGG BRITE Database
Orthology
K00746
Name
chondroitin sulfate N-acetylgalactosaminyltransferase 1/2 [EC:2.4.1.174 2.4.1.175]
References
Reactions
Displaying 1 entry
KEGG Reaction Enzyme Acceptor Product
R05929
Disease
Disease Ontology
Displaying entries 31 - 37 of 37 in total
DO ID Disease Name Source
DOID:4480 achondroplasia
DOID:5672 large intestine cancer
DOID:8689 anorexia nervosa
DOID:8923 skin melanoma
DOID:9256 colorectal cancer
DOID:9521 Laron syndrome
DOID:9744 type 1 diabetes mellitus
The Human Phenotype Ontology
Displaying entries 61 - 69 of 69 in total
HPO ID HPO Term
HP:0007018 Attention deficit hyperactivity disorder
HP:0007165 Periventricular heterotopia
HP:0008070 Sparse hair
HP:0008873 Disproportionate short-limb short stature
HP:0010318 Aplasia/Hypoplasia of the abdominal wall musculature
HP:0010880 Increased nuchal translucency
HP:0011800 Midface retrusion
HP:0100490 Camptodactyly of finger
HP:0200055 Small hand
Displaying all 2 entries
Disease ID Disease Name
OMIM:618870
  • skeletal dysplasia, mild, with joint laxity and advanced bone age
ORPHA:1425
  • Desbuquois dysplasia

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024