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Chromosome Structure Variation : Del(11Irf1-D11Mit23)1Rub deletion, Chr 11, Edward M Rubin 1

Primary Identifier  MGI:3614963 Organism  mouse, laboratory
Chromosome  11 Mgi Type  chromosomal deletion
description  PHENOTYPE: Deletion homozygotes exhibit growth retardation, enlargement of the heart and liver, severe hypertriglyceridemia due to several-fold elevated hepatic secretion of very low density lipoprotein (VLDL) triglycerides, and premature death. [provided by MGI curators]
  • synonyms:
  • del<11>,
  • Del1Rub,
  • Del(11Irf1-Csf2)1Rub,
  • Del(11Irf1-D11Mit23)1Rub,
  • deletion, Chr 11, Edward M Rubin 1

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Involved In Mutations

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Function

Mouse features --> Functions (GO terms)

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications