| Primary Identifier | MGI:3588197 | Organism | mouse, laboratory |
| Chromosome | 12 | NCBI Gene Number | 432677 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0) Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be part of chromatin. Orthologous to human VRTN (vertebrae development associated). PHENOTYPE: Mice homozygous for a null allele exhibit delayed embryonic development, impaires somite formation, failure to initate turning and lethality between E10.5 and E11.5. Mice heterozygous for the allele exhibit kyphosis, decreased thoracic vertebrae numbers and missing rib. [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
