Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55790
Gene name Gene Name - the full gene name approved by the HGNC.
Chondroitin sulfate N-acetylgalactosaminyltransferase 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CSGALNACT1
Synonyms (NCBI Gene) Gene synonyms aliases
CSGalNAcT-1, ChGn, ChGn-1, SDJLABA, beta4GalNAcT
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p21.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes an enzyme that transfers N-acetylglucosamine (GalNAc) to the core tetrasaccharide linker and to elongating chondroitin sulfate chains in proteoglycans. Knockout of the orthologous mouse gene indicates that the protein is necessary for no
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017694 hsa-miR-335-5p Microarray 18185580
MIRT022557 hsa-miR-124-3p Microarray 18668037
MIRT051118 hsa-miR-16-5p CLASH 23622248
MIRT045696 hsa-miR-126-5p CLASH 23622248
MIRT720894 hsa-miR-10a-5p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane NAS 11514575
GO:0000139 Component Golgi membrane TAS
GO:0001958 Process Endochondral ossification IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005794 Component Golgi apparatus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616615 24290 ENSG00000147408
Protein
UniProt ID Q8TDX6
Protein name Chondroitin sulfate N-acetylgalactosaminyltransferase 1 (CsGalNAcT-1) (EC 2.4.1.174) (Chondroitin beta-1,4-N-acetylgalactosaminyltransferase 1) (Beta4GalNAcT-1)
Protein function Transfers 1,4-N-acetylgalactosamine (GalNAc) from UDP-GalNAc to the non-reducing end of glucuronic acid (GlcUA). Required for addition of the first GalNAc to the core tetrasaccharide linker and for elongation of chondroitin chains. Important rol
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05679 CHGN 58 507 Chondroitin N-acetylgalactosaminyltransferase Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitous, with the highest levels in placenta, thyroid, bladder, prostate and adrenal gland. Detected at low levels in the other tissues examined. {ECO:0000269|PubMed:11788602, ECO:0000269|PubMed:12163485, ECO:0000269|PubMed:12446672
Sequence
Sequence length 532
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate
Metabolic pathways
  Chondroitin sulfate biosynthesis
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Skeletal dysplasia, mild, with joint laxity and advanced bone age rs2077140472, rs2054868908 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Dermatitis Atopic dermatitis (moderate to severe) N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Dyslexia Dyslexia N/A N/A GWAS
Hyperlipidemia Familial combined hyperlipidemia defined by Dutch criteria N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Anorexia Nervosa Associate 35703085
Cartilage Diseases Associate 23748413
Cataract Age Related Nuclear Associate 34954695
Congenital Disorders of Glycosylation Associate 31705726
Growth Disorders Associate 31705726
HEM dysplasia Associate 31705726
Intervertebral Disc Degeneration Associate 30148873
Kashin Beck Disease Inhibit 23748413
Language Development Disorders Associate 31705726
Osteoarthritis Associate 15176972