| Primary Identifier | MGI:1289160 | Organism | mouse, laboratory |
| Chromosome | 9 | NCBI Gene Number | 14012 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Acts upstream of or within T cell differentiation in thymus and cell-cell adhesion. Located in plasma membrane. Is expressed in several structures, including branchial arch; epithelium; genitourinary system; gut; and hemolymphoid system. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 111. Orthologous to human MPZL2 (myelin protein zero like 2). PHENOTYPE: Mice homozygous for a targeted mutation exhibit alterations in immune cell percentages in peripheral blood and in spleen. [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
