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Heritable Phenotypic Marker : Rgsc859 RIKEN Genomic Sciences Center (GSC), 859
Primary Identifier  MGI:3807257 Organism  mouse, laboratory
Chromosome  UN Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Mice with a mutation of this gene have a reduced red blood cell count, mean corpuscular volume (MCV) and mean corpuscular hemoglobin content (MCH) and increased red blood cell volume distribution width (RDW) and hemoglobin distribution width (HDW). [provided by MGI curators]
  • synonyms:
  • Rgsc859,
  • RIKEN Genomic Sciences Center (GSC), 859,
  • M100859
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Involved In Mutations

0 Transgenic Expressors

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

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





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