# Solute carrier family 5 (inositol transporters), member 3

> mammalian protein found in Mus musculus

**Wikidata**: [Q21991123](https://www.wikidata.org/wiki/Q21991123)  
**Source**: https://4ort.xyz/entity/solute-carrier-family-5-inositol-transporters-member-3


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9JKZ2)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9JKZ2&geneProductId=UniProtKB:Q9JKZ2)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9JKZ2)
6. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9JKZ2)
7. [Sodium/myo-inositol cotransporter-1 is essential for the development and function of the peripheral nerves](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9JKZ2)
8. [Characterization of the null murine sodium/myo-inositol cotransporter 1 (Smit1 or Slc5a3) phenotype: myo-inositol rescue is independent of expression of its cognate mitochondrial ribosomal protein subunit 6 (Mrps6) gene and of [...]](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9JKZ2&geneProductId=UniProtKB:Q9JKZ2)
9. [SMIT1 haploinsufficiency causes brain inositol deficiency without affecting lithium-sensitive behavior](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9JKZ2&geneProductId=UniProtKB:Q9JKZ2)
10. [Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9JKZ2)
11. [Sodium/myo-inositol cotransporter-1 is essential for the development and function of the peripheral nerves](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9JKZ2&geneProductId=UniProtKB:Q9JKZ2)
12. [Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9JKZ2&geneProductId=UniProtKB:Q9JKZ2)
13. [SMIT1 haploinsufficiency causes brain inositol deficiency without affecting lithium-sensitive behavior](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9JKZ2)
14. [Characterization of the null murine sodium/myo-inositol cotransporter 1 (Smit1 or Slc5a3) phenotype: myo-inositol rescue is independent of expression of its cognate mitochondrial ribosomal protein subunit 6 (Mrps6) gene and of [...]](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9JKZ2)
15. ensembl Release 106