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Protein Coding Gene : Lrrtm2 leucine rich repeat transmembrane neuronal 2

Primary Identifier  MGI:2389174 Organism  mouse, laboratory
Chromosome  18 NCBI Gene Number  107065
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable neurexin family protein binding activity. Acts upstream of or within several processes, including long-term synaptic potentiation; negative regulation of receptor internalization; and positive regulation of synapse assembly. Predicted to be located in excitatory synapse and membrane. Predicted to be active in several cellular components, including Schaffer collateral - CA1 synapse; hippocampal mossy fiber to CA3 synapse; and postsynaptic density membrane. Is expressed in neural tube and neural tube lateral wall. Orthologous to human LRRTM2 (leucine rich repeat transmembrane neuronal 2).
PHENOTYPE: When conditionally deleted in addition to Lrrtm1, mice homozygous for a conditional allele exhibit impaired basal AMPA receptor transmission and LTP. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA C630011A14 gene,
  • expressed sequence AI851755,
  • C630011A14Rik,
  • leucine rich repeat transmembrane neuronal 2,
  • BB129880,
  • AI851755,
  • MGI:2147387,
  • Lrrtm2,
  • expressed sequence BB129880,
  • mKIAA0416,
  • MGI:2147278

Features --> Cross References

Genome

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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

3 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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