ATP9A

Last updated
ATP9A
Identifiers
Aliases ATP9A , ATPIIA, ATPase phospholipid transporting 9A (putative)
External IDs OMIM: 609126 MGI: 1330826 HomoloGene: 69194 GeneCards: ATP9A
Gene location (Human)
Ideogram human chromosome 20.svg
Chr. Chromosome 20 (human) [1]
Human chromosome 20 ideogram.svg
HSR 1996 II 3.5e.svg
Red rectangle 2x18.png
Band 20q13.2Start51,596,514 bp [1]
End51,768,390 bp [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006045

NM_001289445
NM_001289446
NM_015731
NM_001354977
NM_001354978

RefSeq (protein)

NP_006036

NP_001276374
NP_001276375
NP_056546
NP_001341906
NP_001341907

Location (UCSC) Chr 20: 51.6 – 51.77 Mb Chr 2: 168.63 – 168.74 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

ATPase phospholipid transporting 9A (putative) is a protein that in humans is encoded by the ATP9A gene. [5]


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References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000054793 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000027546 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: ATPase phospholipid transporting 9A (putative)" . Retrieved 2016-10-04.

Further reading