| Primary Identifier | MGI:1915508 | Organism | mouse, laboratory |
| Chromosome | 19 | NCBI Gene Number | 107373 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to enable single-stranded DNA binding activity. Predicted to be involved in DNA metabolic process; negative regulation of viral genome replication; and protein autoprocessing. Predicted to act upstream of or within DNA repair. Predicted to be located in cytoplasm; fibrillar center; and nucleoplasm. Predicted to be part of chromatin. Predicted to be active in nucleus. Is expressed in alimentary system; brain ventricular layer; liver lobe; and orbito-sphenoid. Human ortholog(s) of this gene implicated in Kenny-Caffey syndrome type 2. Orthologous to human FAM111A (FAM111 trypsin like peptidase A). PHENOTYPE: Mice homozygous for a null allele exhibit normal electrolyte homeostasis and bone phenotype. [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
