| Primary Identifier | MGI:1916092 | Organism | mouse, laboratory |
| Chromosome | 17 | NCBI Gene Number | 68842 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0) Predicted to be located in cytoplasm. Is expressed in incisor; intestine smooth muscle circular layer; nervous system; sensory organ; and vibrissa. Orthologous to human TULP4 (TUB like protein 4). PHENOTYPE: Mice homozygous for a null allele exhibit perinatal lethality and multiple malformations during embryonic development, including severe cardiovascular and endo-/exocrine gland defects. Heterozygotes have developmental defects in several organ systems but show normal survival and a trend for increased body weight in adulthood. [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
