| Primary Identifier | MGI:97584 | Organism | mouse, laboratory |
| Chromosome | 17 | NCBI Gene Number | 18712 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Enables ATP binding activity; manganese ion binding activity; and protein serine/threonine kinase activity. Involved in several processes, including positive regulation of brown fat cell differentiation; protein stabilization; and regulation of hematopoietic stem cell proliferation. Predicted to be located in cytosol; nuclear lumen; and plasma membrane. Predicted to be active in cytoplasm. Is expressed in several structures, including brain; genitourinary system; primitive streak; sensory organ; and yolk sac. Orthologous to human PIM1 (Pim-1 proto-oncogene, serine/threonine kinase). PHENOTYPE: Mice homozygous for disruptions in this gene have abnormally small erythrocytes but are otherwise phenotypically normal. [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
