# ATPase, aminophospholipid transporter-like, class I, type 8A, member 2

> mammalian protein found in Mus musculus

**Wikidata**: [Q21983516](https://www.wikidata.org/wiki/Q21983516)  
**Source**: https://4ort.xyz/entity/atpase-aminophospholipid-transporter-like-class-i-type-8a-member-2


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P98200)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P98200)
5. [Mutations in a P-type ATPase gene cause axonal degeneration](http://www.ebi.ac.uk/QuickGO/annotations?protein=P98200&geneProductId=UniProtKB:P98200)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P98200&geneProductId=UniProtKB:P98200)
7. [Mutations in a P-type ATPase gene cause axonal degeneration](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P98200)
8. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P98200)
9. [Phospholipid flippase ATP8A2 is required for normal visual and auditory function and photoreceptor and spiral ganglion cell survival](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P98200)
10. [Genetic and age related models of neurodegeneration in mice: dystrophic axons](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P98200)
11. [Genetic and age related models of neurodegeneration in mice: dystrophic axons](http://www.ebi.ac.uk/QuickGO/annotations?protein=P98200&geneProductId=UniProtKB:P98200)
12. [P4-ATPase ATP8A2 acts in synergy with CDC50A to enhance neurite outgrowth](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P98200)
13. ensembl Release 106
14. Transporter Classification database