| Primary Identifier | MGI:3612246 | Organism | mouse, laboratory |
| Chromosome | 10 | NCBI Gene Number | 432478 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Enables serine-type peptidase activity. Acts upstream of or within plasminogen activation. Predicted to be located in plasma membrane. Used to study autism spectrum disorder. Orthologous to human TMPRSS9 (transmembrane serine protease 9). PHENOTYPE: Mice homozygous for a null allele show decreased social interest and social recognition and aged females show a borderline recognition memory deficit. [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
