| Primary Identifier | MGI:1338822 | Organism | mouse, laboratory |
| Chromosome | 2 | NCBI Gene Number | 14007 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables lncRNA binding activity. Acts upstream of or within mRNA splice site recognition. Located in cytoplasm and nucleus. Is expressed in several structures, including central nervous system; foregut; hemolymphoid system gland; limb; and urinary system. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 97. Orthologous to human CELF2 (CUGBP Elav-like family member 2). PHENOTYPE: Mice homozygous for a knock-out allele die neonatally and postnatally with reduced axon extension in DRG explants. [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
