| Primary Identifier | MGI:1914475 | Organism | mouse, laboratory |
| Chromosome | 3 | NCBI Gene Number | 67225 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable U12 snRNA binding activity and pre-mRNA intronic binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be part of U12-type spliceosomal complex. Is expressed in central nervous system; dorsal root ganglion; nose; trigeminal nerve; and urinary system. Human ortholog(s) of this gene implicated in combined pituitary hormone deficiency. Orthologous to human RNPC3 (RNA binding region (RNP1, RRM) containing 3). PHENOTYPE: Embryos homozygous for a knock-out allele fail to develop beyond the morula stage and die before implantation. [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
