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Heritable Phenotypic Marker : Cbll cerebelless

Primary Identifier  MGI:3771554 Organism  mouse, laboratory
Chromosome  2 Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Mice homozygous for an intergenic deletion caused by random insertion of a transgene exhibit decreased body size, tremors, ataxia, impaired coordination, absent cerebellar cortex, failure of GABAergic neuron production, and loss of external germinal layer, pontine and olivary nuclei. [provided by MGI curators]
  • synonyms:
  • Cbll,
  • cerebelless

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