| Primary Identifier | MGI:2143652 | Organism | mouse, laboratory |
| Chromosome | 10 | NCBI Gene Number | 103266 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to be located in membrane. Orthologous to human TMEM263 (transmembrane protein 263). PHENOTYPE: Mice homozygous for a null allele exhibit severe postnatal growth failure, proportional dwarfism, and skeletal dysplasia with reduced bone mass and growth plate length. Serum calcium, insulin and glucose levels are reduced. [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
