| Primary Identifier | MGI:1929772 | Organism | mouse, laboratory |
| Chromosome | 5 | NCBI Gene Number | 65254 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides. Predicted to be involved in negative regulation of dendrite morphogenesis. Predicted to act upstream of or within axon guidance. Located in cytoplasm; dendrite; and neuronal cell body. Is active in glutamatergic synapse. Is expressed in several structures, including nervous system; olfactory epithelium; and retina. Human ortholog(s) of this gene implicated in Ritscher-Schinzel syndrome. Orthologous to human DPYSL5 (dihydropyrimidinase like 5). PHENOTYPE: Mice homozygous for a knock-out allele exhibit limb grasping, abnormal Purkinje morphology, absent long term depression, and no response to BDNF. [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
