1. Gene
  2. HS3ST3B1 - heparan sulfate-glucosamine 3-sulfotransferase 3B1 Gene

HS3ST3B1 - heparan sulfate-glucosamine 3-sulfotransferase 3B1 Gene

Homo sapiens

Also known as 3OST3B1; 3-OST-3B; h3-OST-3B

Gene ID: 9953 | Gene type: protein coding

About HS3ST3B1

Cytogenetic location: 17p12 Genomic coordinates (GRCh38): 17:14,301,081-14,349,404 (from NCBI)

This gene has 2 transcripts (splice variants), 471 orthologues and 10 paralogues. Broad expression in liver (RPKM 6.8), lymph node (RPKM 3.1) and 21 other tissues.

Summary

The protein encoded by this gene is a type II integral membrane protein that belongs to the 3-O-sulfotransferases family. These proteins catalyze the addition of sulfate groups at the 3-OH position of glucosamine in heparan sulfate. The substrate specificity of individual members of the family is based on prior modification of the heparan sulfate chain, thus allowing different members of the family to generate binding sites for different proteins on the same heparan sulfate chain. Following treatment with a histone deacetylase inhibitor, expression of this gene is activated in a pancreatic cell line. The increased expression results in promotion of the epithelial-mesenchymal transition. In addition, the modification catalyzed by this protein allows herpes simplex virus membrane fusion and penetration. A very closely related homolog with an almost identical sulfotransferase domain maps less than 1 Mb away. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]

HS3ST3B1 Products(1)

mRNA Protein Name
NM_006041.3 NP_006032.1 heparan sulfate glucosamine 3-O-sulfotransferase 3B1
Protein Preferred Names Protein Names

heparan sulfate glucosamine 3-O-sulfotransferase 3B1

heparan sulfate (glucosamine) 3-O-sulfotransferase 3B1

Related Diseases

Diseases Alias
Herpes Simplex

Herpes Simplex Infections

Herpesvirus Hominis Disease

Herpes Simplex Disease

Herpesviral Infection Due To Herpes Simplex

Infections Due To Simplex Virus

Herpes Nos

Dihydropyrimidinase Deficiency

Dihydropyrimidinuria

Dpys Deficiency

Dph Deficiency

DPYSD

Dihydrouracil Amidohydrolase Deficiency

Dihydropyrimidinuria Due To Dpys Deficiency

Overhydrated Hereditary Stomatocytosis

Ohs

Potassium Sodium Disorder Of Erythrocyte

OHST

Stomatocytosis I

Potassium-Sodium Disorder Of Erythrocyte

Stomatocytosisiohst

Hereditary, Overhydrated, Cation-Leak Stomatocytosis

Overhydrated Cation Leak Stomatocytosis

Stomatocytosis, Overhydrated Hereditary

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 HS3ST3B1 MGD MGI:1333853
Rattus norvegicus HS3ST3B1 RGD RGD:1307326