| Primary Identifier | MGI:1919709 | Organism | mouse, laboratory |
| Chromosome | X | NCBI Gene Number | 72459 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to enable RNA binding activity; chromatin-protein adaptor activity; and poly-ADP-D-ribose modification-dependent protein binding activity. Predicted to be involved in U2-type prespliceosome assembly; double-strand break repair via homologous recombination; and protein localization to site of double-strand break. Predicted to act upstream of or within DNA repair; RNA splicing; and mRNA processing. Predicted to be located in nucleoplasm. Predicted to be part of U2 snRNP and U2-type spliceosomal complex. Predicted to be active in site of double-strand break. Is expressed in several structures, including limb and nervous system. Orthologous to human HTATSF1 (HIV-1 Tat specific factor 1). PHENOTYPE: Mice homozygous for a conditional allele activated in embryonic stem cells exhibit reduced pluripotency. [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
