| Primary Identifier | MGI:1923760 | Organism | mouse, laboratory |
| Chromosome | 15 | NCBI Gene Number | 76510 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0) Acts upstream of or within neuron differentiation. Located in cytoplasm. Is expressed in brain. Used to study intellectual disability. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 13. Orthologous to human TRAPPC9 (trafficking protein particle complex subunit 9). PHENOTYPE: Homozygous null mice exhibit decreased brain size, brain structural malformations, a wide range of behavioral deficits, and increased body weight. [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
