| Primary Identifier | MGI:1914116 | Organism | mouse, laboratory |
| Chromosome | 19 | NCBI Gene Number | 66866 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to be located in cytosol. Is expressed in several structures, including central nervous system; cranial nerve; egg cylinder; embryo endoderm; and incisor. Orthologous to human NHLRC2 (NHL repeat containing 2). PHENOTYPE: Mice homozygous for a knock-out allele exhibit abnormal trophoblast layer formation and complete embryonic lethality during organogenesis with a failure to gastrulate. Mice compound heterozygous for a KO allele and a human disease-associated point mutation show no phenotype but show a possible effect on RNA homeostasis in neurons. [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
