| Primary Identifier | MGI:2686277 | Organism | mouse, laboratory |
| Chromosome | 7 | NCBI Gene Number | 210094 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to be located in extracellular region. Is expressed in central nervous system; peripheral nervous system ganglion; and sensory organ. Orthologous to human IGLON5 (IgLON family member 5). PHENOTYPE: Homozygous null males show subtle alterations in motor coordination and balance, have depressive-like behavior and excessive nest-building, enlarged seminal vesicle and lymph nodes, and abnormal liver. Females are hyperactive, show enlarged kidney and spleen, and abnormal skin and eye morphology. [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
