| Primary Identifier | MGI:1918816 | Organism | mouse, laboratory |
| Chromosome | 9 | NCBI Gene Number | 71566 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Involved in postsynaptic modulation of chemical synaptic transmission. Is active in postsynaptic membrane. Is expressed in brain. Human ortholog(s) of this gene implicated in short bowel syndrome. Orthologous to human CLMP (CXADR like membrane protein). PHENOTYPE: Mice homozygous for a targeted null allele exhibit reduced viability, bilateral hydronephrosis, increased mean systolic blood pressure, and exhibit several blood chemistry and neurological anomalies. Null mice are samller than controls. [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
