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Protein Coding Gene : Carmil2 capping protein regulator and myosin 1 linker 2

Primary Identifier  MGI:2685431 Organism  mouse, laboratory
Chromosome  8 NCBI Gene Number  234695
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable phospholipid binding activity. Acts upstream of or within several processes, including T cell receptor signaling pathway; positive regulation of T cell activation; and positive regulation of cytokine production. Located in cell-cell junction; cytoplasm; and immunological synapse. Part of F-actin capping protein complex. Human ortholog(s) of this gene implicated in immunodeficiency 58. Orthologous to human CARMIL2 (capping protein regulator and myosin 1 linker 2).
PHENOTYPE: Mice homozygous for a knock-out or ENU-induced allele exhibit decreased regulatory T cells and reduced proliferative and IL2-secretion response to anti-CD3 and anti-CD28 antibodies. [provided by MGI curators]
  • synonyms:
  • Rltpr,
  • Gm585,
  • D130029J02Rik,
  • RIKEN cDNA D130029J02 gene,
  • RGD motif, leucine rich repeats, tropomodulin domain and proline-rich containing,
  • capping protein regulator and myosin 1 linker 2,
  • gene model 585, (NCBI),
  • Carmil2

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Genome

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Canonical gene --> CDSs in specific strains.

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Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

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Mouse features --> Functions (GO terms)

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