| Primary Identifier | MGI:107708 | Organism | mouse, laboratory |
| Chromosome | 18 | NCBI Gene Number | 268996 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable nuclear receptor coactivator activity. Acts upstream of or within several processes, including ephrin receptor signaling pathway; microtubule cytoskeleton organization; and neuronal stem cell population maintenance. Located in microtubule cytoskeleton. Part of SWI/SNF complex and npBAF complex. Is expressed in cerebral cortex subventricular zone; cerebral cortex ventricular layer; ovary; and primary sex cord. Human ortholog(s) of this gene implicated in synovial sarcoma. Orthologous to human SS18 (SS18 subunit of BAF chromatin remodeling complex). PHENOTYPE: Homozygous mutation of this gene results in early gestational lethality and embryonic growth arrest with placental failure caused by impaired placental vascularization and chorioallantoic fusion. [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
