SLC35F3 - solute carrier family 35 member F3 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 148641

About SLC35F3

This gene has 2 transcripts (splice variants), 213 orthologues and 1 paralogue. Biased expression in brain (RPKM 3.2), adrenal (RPKM 0.5) and 8 other tissues.

Summary

Involved in thiamine transport. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC35F3 Products (2)

mRNA Protein Name
NM_001300845.2 NP_001287774.1 putative thiamine transporter SLC35F3 isoform 2
NM_173508.4 NP_775779.1 putative thiamine transporter SLC35F3 isoform 1

Gene Ontology

  • Biological Process
Biological Process GO Annotation Evidence References Source
involved in thiamine transport IDA
IDA: Inferred from direct assay
24509276 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC35F3 Protein Structure

EamA

EamA: EamA-like transporter family (159 - 222)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 421 a.a.
Protein Preferred Names Protein Names

putative thiamine transporter SLC35F3

Related Diseases

Diseases Alias
Dry Beriberi
Wet Beriberi
Beriberi

  • Thiamine Deficiency

  • Vitamin B1 Deficiency

  • Aneurin Deficiency

  • Thiamine Vitamin Deficiency

  • Beriberi Nos

  • Beriberi Due To Vitamin B1 Deficiency

  • Beriberi Due To Thiamine Vitamin Deficiency

  • Kakkè
Thiamine Deficiency Disease
Diverticulitis Of Colon

  • Colonic Diverticular Disease

  • Diverticulitis, Colonic

  • Diverticular Disease Of Colon
Mitochondrial Trifunctional Protein Deficiency

  • Tfp Deficiency

  • MTPD

  • Trifunctional Protein Deficiency

  • Trifunctional Protein Deficiency With Myopathy And Neuropathy

  • Tfpd

  • Familial Hypertrophic Cardiomyopathy

  • Cardiomyopathy Familial Hypertrophic

  • Familial Hcm

  • Heritable Hypertrophic Cardiomyopathy

  • Mtp Deficiency

  • Tpa Deficiency

  • Trifunctional Protein Deficiency, Type 2

  • Abetalipoproteinemia
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13207 SLC35F3 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus SLC35F3 MGD MGI:2444426
Canis familiaris SLC35F3 VGNC VGNC:46377
Bos taurus SLC35F3 VGNC VGNC:34833
Rattus norvegicus SLC35F3 RGD RGD:1589548
Macaca mulatta SLC35F3 VGNC VGNC:77566
Felis catus SLC35F3 VGNC VGNC:82508
Others SLC35F3 NCBI