2. Gene
  3. Slc35d1 - solute carrier family 35 member D1 Gene

Slc35d1 - solute carrier family 35 member D1 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Rattus norvegicus
Gene ID: 298280 | Gene type: protein coding

About Slc35d1

Summary

Predicted to enable antiporter activity and pyrimidine nucleotide-sugar transmembrane transporter activity. Predicted to be involved in UDP-N-acetylgalactosamine transmembrane transport; UDP-N-acetylglucosamine transmembrane transport; and UDP-glucuronic acid transmembrane transport. Predicted to act upstream of or within chondroitin sulfate biosynthetic process; embryonic skeletal system development; and pyrimidine nucleotide-sugar transmembrane transport. Predicted to be located in endoplasmic reticulum. Predicted to be active in Golgi apparatus. Human ortholog(s) of this gene implicated in schneckenbecken dysplasia. Orthologous to human SLC35D1 (solute carrier family 35 member D1). [provided by Alliance of Genome Resources, Apr 2022]

Slc35d1 Products(1)

mRNA Protein Name
NM_001106668.2 NP_001100138.1 UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter
Protein Preferred Names Protein Names

UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter

solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1

solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS13201 SLC35D1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc35d1 NCBI NCBI:23169