| Primary Identifier | MGI:1915677 | Organism | mouse, laboratory |
| Chromosome | 2 | NCBI Gene Number | 68427 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to enable protein homodimerization activity and zinc ion transmembrane transporter activity. Involved in several processes, including brown fat cell differentiation; intracellular zinc ion homeostasis; and zinc ion transmembrane transport. Located in Golgi apparatus and perinuclear region of cytoplasm. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome and Ehlers-Danlos syndrome spondylodysplastic type 3. Orthologous to human SLC39A13 (solute carrier family 39 member 13). PHENOTYPE: Mice homozygous for disruption of this gene display skeletal abnormalities and dental abnormalities. [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
