| Primary Identifier | MGI:5311361 | Organism | mouse, laboratory |
| Chromosome | UN | Mgi Type | heritable phenotypic marker |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Used to study Williams-Beuren syndrome. PHENOTYPE: More than one mutation in this ENU line results in a discernible phenotype in a homozygous recessive screen. At least two segregating phenotype groups are identified. [provided by MGI curators] |
Features --> Cross References
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
