| Primary Identifier | MGI:1355295 | Organism | mouse, laboratory |
| Chromosome | X | NCBI Gene Number | 50887 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Enables chromatin binding activity. Acts upstream of or within chromatin organization; glutathione metabolic process; and regulation of transcription by RNA polymerase II. Located in nucleoplasm. Is expressed in several structures, including 1st branchial arch; brain; genitourinary system; gut gland; and hemolymphoid system gland. Orthologous to human HMGN5 (high mobility group nucleosome binding domain 5). PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased prepulse inhibition, abnormal erythrocyte cell number, abnormal glucose tolerance, decreased granulocyte, increased CD8+ T cells, increased IgA, decreased IgE and abnormal respiration. [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
