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Protein Coding Gene : Rtn1 reticulon 1
Primary Identifier  MGI:1933947 Organism  mouse, laboratory
Chromosome  12 NCBI Gene Number  104001
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to be involved in endoplasmic reticulum tubular network formation; negative regulation of amyloid-beta formation; and nervous system development. Located in dendrite; endoplasmic reticulum; and neuronal cell body. Is expressed in several structures, including genitourinary system; immune system; nervous system; neural retina; and skin. Orthologous to human RTN1 (reticulon 1).
PHENOTYPE: Mice homozygous for a null allele are viable with no gross abnormalities. [provided by MGI curators]
  • synonyms:
  • Rtn1-a,
  • reticulon 1,
  • 0710005K15Rik,
  • RIKEN cDNA 4930441F12 gene,
  • MGI:1926049,
  • RIKEN cDNA 0710005K15 gene,
  • MGC:40985,
  • Rtn1-c,
  • expressed sequence R75279,
  • 4930441F12Rik,
  • MGI:1913343,
  • Rtn1-b,
  • Nsp,
  • MGI:2145135,
  • R75279,
  • Rtn1
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Features --> Cross References

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Sequence Feature Displayer

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1 Involved In Mutations

Trail: ProteinCodingGene

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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

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Genes/Features --> Phenotypes (MP terms)

Disease

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