| Primary Identifier | MGI:1345622 | Organism | mouse, laboratory |
| Chromosome | 4 | NCBI Gene Number | 24060 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Enables CMP-N-acetylneuraminate transmembrane transporter activity and antiporter activity. Involved in CMP-N-acetylneuraminate biosynthetic process; CMP-N-acetylneuraminate transmembrane transport; and N-acetylneuraminate metabolic process. Located in Golgi membrane. Is expressed in several structures, including genitourinary system; liver; lung; retina; and spleen. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIf. Orthologous to human SLC35A1 (solute carrier family 35 member A1). PHENOTYPE: Homozygous mutation of this gene results in lethality before weaning. [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
