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

ATP9A
Identifiers
AliasesATP9A, ATPIIA, ATPase phospholipid transporting 9A (putative)
External IDsOMIM: 609126 MGI: 1330826 HomoloGene: 69194 GeneCards: ATP9A
Gene location (Human)
Chromosome 20 (human)
Chr.Chromosome 20 (human)[1]
Chromosome 20 (human)
Genomic location for ATP9A
Genomic location for ATP9A
Band20q13.2Start51,596,514 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 MbChr 2: 168.63 – 168.74 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse


ReferencesEdit

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000054793 - Ensembl, May 2017
  2. ^ a b c 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 readingEdit