1. Gene
  2. CHST10 - carbohydrate sulfotransferase 10 Gene

CHST10 - carbohydrate sulfotransferase 10 Gene

Homo sapiens

Also known as HNK1ST; HNK-1ST

Gene ID: 9486 | Gene type: protein coding

About CHST10

Cytogenetic location: 2q11.2 Genomic coordinates (GRCh38): 2:100,391,860-100,417,668 (from NCBI)

This gene has 12 transcripts (splice variants), 201 orthologues and 6 paralogues. Broad expression in brain (RPKM 10.4), endometrium (RPKM 4.2) and 21 other tissues.

Summary

This protein encoded by this gene transfers sulfate to the C-3 hydroxyl of terminal glucuronic acid of protein- and lipid-linked oligosaccharides. This protein was first identified as a sulfotransferase that acts on the human natural killer-1 (HNK-1) glycan; HNK-1 is a carbohydrate involved in neurodevelopment and synaptic plasticity.[provided by RefSeq, Feb 2011]

CHST10 Products(1)

mRNA Protein Name
NM_004854.5 NP_004845.1 carbohydrate sulfotransferase 10 precursor

CHST10 Protein Structure

Sulfotransfer_2

Sulfotransfer_2: Sulfotransferase family (112 - 349)

  • 0
  • 100
  • 200
  • 300
  • 356 a.a.
Protein Preferred Names Protein Names

carbohydrate sulfotransferase 10

HNK-1 sulfotransferase

Recombinant CHST10 Proteins

Cat. No. Product Name Accession Purity
HY-P79210 CHST10 Protein, Human (CHO, His) O43529 (P32-N356) ≥95%

Related Diseases

Diseases Alias
Retinitis Pigmentosa 33

RP33

Retinitis Pigmentosa, Type 33

Walker-Warburg Syndrome

Hard Syndrome

Walker-Warburg Congenital Muscular Dystrophy

Cerebroocular Dysplasia-Muscular Dystrophy Syndrome

Cod-Md Syndrome

Chemke Syndrome

Hydrocephalus, Agyria And Retinal Dysplasia

Cerebroocular Dysgenesis

Cerebroocular Dysplasia Muscular Dystrophy Syndrome

Hard +/- E Syndrome

Pagon Syndrome

Warburg Syndrome

Hydrocephalus, Agyria, And Retinal Dysplasia

Mddga

Muscular Dystrophy-Dystroglycanopathy , Type A

Muscular Dystrophy-Dystroglycanopathy [With Brain And Eye Anomalies], Type A

Hydrocephalus-Agyria-Retinal Dysplasia Syndrome

Wws

Dystrophy, Muscular, Dystroglycanopathy, Type A

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus CHST10 MGD MGI:2138283
Canis familiaris CHST10 VGNC VGNC:39250
Felis catus CHST10 VGNC VGNC:60888
Bos taurus CHST10 VGNC VGNC:27338
Rattus norvegicus CHST10 RGD RGD:621216
Macaca mulatta CHST10 VGNC VGNC:71052