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MGI:Slc5a3

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Slc5a3 ( synonyms: Smit1 )
Protein Name(s) solute carrier family 5 (inositol transporters), member 3,
External Links
MGI MGI:1858226

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0005215

transporter activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001734
InterPro:IPR018212

F

From MGI

GO:0006020

inositol metabolic process

MGI:MGI:3654617
PMID:16644257[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2663787

P

From MGI

GO:0006020

inositol metabolic process

MGI:MGI:3812279
PMID:18675571[2]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2663787

P

From MGI

GO:0006810

transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0813

P

From MGI

GO:0006810

transport

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001734
InterPro:IPR018212
InterPro:IPR019900

P

From MGI

GO:0006811

ion transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0406

P

From MGI

GO:0006814

sodium ion transport

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0739

P

From MGI

GO:0007422

peripheral nervous system development

MGI:MGI:3607889
PMID:16174787[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3609547

P

From MGI

GO:0015293

symporter activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0769

F

From MGI

GO:0015798

myo-inositol transport

MGI:MGI:2662670
PMID:12582158[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2663787

P

From MGI

GO:0015798

myo-inositol transport

MGI:MGI:3607889
PMID:16174787[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3609547

P

From MGI

GO:0016020

membrane

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0472

C

From MGI

GO:0016020

membrane

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001734
InterPro:IPR018212
InterPro:IPR019900

C

From MGI

GO:0016021

integral to membrane

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0812

C

From MGI

GO:0043576

regulation of respiratory gaseous exchange

MGI:MGI:2662670
PMID:12582158[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2663787

P

From MGI

GO:0055085

transmembrane transport

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR001734

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. Shaldubina A et al. (2006) SMIT1 haploinsufficiency causes brain inositol deficiency without affecting lithium-sensitive behavior. Mol Genet Metab 88: 384-8 PubMed GONUTS page
  2. Buccafusca R et al. (2008) 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 phosphatidylinositol levels in neonatal brain. Mol Genet Metab 95: 81-95 PubMed GONUTS page
  3. 3.0 3.1 Chau JF et al. (2005) Sodium/myo-inositol cotransporter-1 is essential for the development and function of the peripheral nerves. FASEB J 19: 1887-9 PubMed GONUTS page
  4. 4.0 4.1 Berry GT et al. (2003) Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea. J Biol Chem 278: 18297-302 PubMed GONUTS page
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