Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) Kits ELISA

SLC35A3 encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane. De plus, nous expédions Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 Anticorps (17) et Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 Protéines (4) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
Anti-Souris SLC35A3 SLC35A3 229782 Q8R1T4
Anti-Humain SLC35A3 SLC35A3 23443 Q9Y2D2
Anti-Rat SLC35A3 SLC35A3 310808 Q6AXR5
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Plus Kits ELISA pour Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 partenaires d'interaction

Human Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) interaction partners

  1. UDP-galactose (Montrer B4GALT1 Kits ELISA) (SLC35A2 (Montrer SLC35A2 Kits ELISA)) and UDP-N-acetylglucosamine (Montrer MGAT4B Kits ELISA) (SLC35A3) Transporters Form Glycosylation-related Complexes with Mannoside Acetylglucosaminyltransferases (Mgats).

  2. Identified deleterious mutations in SLC35A3 in eight patients from a large kindred, who suffered from autism spectrum disorder, arthrogryposis and epilepsy.

  3. The data further supports the hypothesis that UGT (Montrer SLC35A2 Kits ELISA) and NGT cooperate in the UDP-Gal (Montrer B4GALT1 Kits ELISA) delivery for glycosyltransferases located in the Golgi apparatus.

  4. A mutation in the SLC35A3 gene is associated with vertebral malformations in cattle. A missense mutation likely effects signal transduction which relies on glycosylation.

  5. SLC35A3 is an unlikely candidate for the pathogenesis of vertebral malformations because no mutation was found in this cohort study.

Cow (Bovine) Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) interaction partners

  1. A defective SLC35A3 gene is associated with severe axial skeletal deformities, symmetric arthrogryposis of the lower limb joints, craniofacial dysmorphism, and cardiac anomalies.

Solute Carrier Family 35 (UDP-N-Acetylglucosamine (UDP-GlcNAc) Transporter), Member A3 (SLC35A3) profil antigène

Antigen Summary

This gene encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane. In cattle, a missense mutation in this gene causes complex vertebral malformation. Alternative splicing results in multiple transcript variants.

Gene names and symbols associated with SLC35A3

  • solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 (Slc35a3) anticorps
  • solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3 (SLC35A3) anticorps
  • solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3 (Slc35a3) anticorps
  • 2310050P13Rik anticorps

Protein level used designations for SLC35A3

UDP-N-acetylglucosamine transporter , golgi UDP-GlcNAc transporter , solute carrier family 35 member A3 , solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member 3 , UDP N-acetylglucosamine transporter , solute carrier family 35 member 3

GENE ID SPECIES
229782 Mus musculus
23443 Homo sapiens
442991 Canis lupus familiaris
520918 Bos taurus
310808 Rattus norvegicus
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