| Primary Identifier | MGI:107672 | Organism | mouse, laboratory |
| Chromosome | X | NCBI Gene Number | 14758 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to be a structural constituent of myelin sheath. Involved in negative regulation of protein localization to cell surface and negative regulation of serotonin uptake. Located in membrane raft and plasma membrane. Is expressed in central nervous system; genitourinary system; and retina. Orthologous to human GPM6B (glycoprotein M6B). PHENOTYPE: Mice null for this gene display axon-myelin interface irregularities but do not show motor function defects. [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
