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Protein Coding Gene : Slc20a1 solute carrier family 20, member 1

Primary Identifier  MGI:108392 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  20515
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable high-affinity phosphate:sodium symporter activity. Acts upstream of or within biomineral tissue development. Located in plasma membrane. Is expressed in several structures, including alimentary system; genitourinary system; nervous system; submandibular gland primordium; and yolk sac. Orthologous to human SLC20A1 (solute carrier family 20 member 1).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit mid-gestation lethality associated with abnormal vitelline vasculature, growth retardation, and anemia. [provided by MGI curators]
  • synonyms:
  • MGI:2139020,
  • Glvr-1,
  • solute carrier family 20, member 1,
  • PiT-1,
  • MGD-MRK-10164,
  • expressed sequence AI607883,
  • MGD-MRK-37434,
  • AI607883,
  • gibbon ape leukemia virus receptor 1,
  • Glvr1,
  • Slc20a1,
  • MGD-MRK-10163

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For