ATP13A4
Probable cation-transporting ATPase 13A4
Also known as: AT134_HUMAN, DKFZp761I1011, FLJ37958
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q4VNC1
- Gene
- ATP13A4
- Ensembl
- ENSG00000127249
- Chromosome
- 3
- Canonical length
- 1196 aa
- Protein class
- Disease related genes, Potential drug targets, Predicted membrane proteins, Transporters
OverviewNCBI Gene
Predicted to enable ATPase-coupled monoatomic cation transmembrane transporter activity and polyamine transmembrane transporter activity. Predicted to be involved in intracellular calcium ion homeostasis and polyamine transmembrane transport. Predicted to be located in early endosome membrane and recycling endosome membrane. Predicted to be active in endoplasmic reticulum membrane and late endosome membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1196 residues, UniProt reviewed canonical sequence.
>Q4VNC1|ATP13A4
1 MGHFEKGQHA LLNEGEENEM EIFGYRTQGC RKSLCLAGSI FSFGILPLVF YWRPAWHVWA
61 HCVPCSLQEA DTVLLRTTDE FQIYSWKKVI WIYLSALNSA FGLTPDHPLM TDEEYIINRA
121 IRKPDLKVRC IKVQKIRYVW NYLEGQFQKI GSLEDWLSSA KIHQKFGSGL TREEQEIRRL
181 ICGPNTIDVE VTPIWKLLIK EVLNPFYIFQ LFSVCLWFSE DYKEYAFAII IMSIISISLT
241 VYDLREQSVK LHHLVESHNS ITVSVCGRKA GVQELESRVL VPGDLLILTG NKVLMPCDAV
301 LIEGSCVVDE GMLTGESIPV TKTPLPKMDS SVPWKTQSEA DYKRHVLFCG TEVIQAKAAC
361 SGTVRAVVLQ TGFNTAKGDL VRSILYPKPV NFQLYRDAIR FLLCLVGTAT IGMIYTLCVY
421 VLSGEPPEEV VRKALDVITI AVPPALPAAL TTGIIYAQRR LKKRGIFCIS PQRINVCGQL
481 NLVCFDKTGT LTRDGLDLWG VVSCDRNGFQ EVHSFASGQA LPWGPLCAAM ASCHSLILLD
541 GTIQGDPLDL KMFEATTWEM AFSGDDFHIK GVPAHAMVVK PCRTASQVPV EGIAILHQFP
601 FSSALQRMTV IVQEMGGDRL AFMKGAPERV ASFCQPETVP TSFVSELQIY TTQGFRVIAL
661 AYKKLENDHH ATTLTRETVE SDLIFLGLLI LENRLKEETK PVLEELISAR IRTVMITGDN
721 LQTAITVARK SGMVSESQKV ILIEANETTG SSSASISWTL VEEKKHIMYG NQDNYINIRD
781 EVSDKGREGS YHFALTGKSF HVISQHFSSL LPKILINGTI FARMSPGQKS SLVEEFQKLD
841 YFVGMCGDGA NDCGALKMAH VGISLSEQEA SVASPFTSKT PNIECVPHLI KEGRAALVTS
901 FCMFKYMALY SMIQYVGVLL LYWETNSLSN YQFLFQDLAI TTLIGVTMNL NGAYPKLVPF
961 RPAGRLISPP LLLSVIFNIL LSLAMHIAGF ILVQRQPWYS VEIHSACTVQ NESISELTMS
1021 PTAPEKMESN STFTSFENTT VWFLGTINCI TVALVFSKGK PFRQPTYTNY IFVLVLIIQL
1081 GVCLFILFAD IPELYRRLDL LCTPVLWRAS IVIMLSLNFI VSLVAEEAVI ENRALWMMIK
1141 RCFGYQSKSQ YRIWQRDLAN DPSWPPLNQT SHSDMPECGR GVSYSNPVFE SNEEQLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATP13A4 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Other membrane
- Secreted
- No
- Transmembrane segments
- 10
- Mean surface accessibility (rSASA)
- 0.25
- Highest tissue expression
- 61 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 61 nTPM
- parathyroid gland: 55 nTPM
- thyroid gland: 49 nTPM
- lung: 26 nTPM
- choroid plexus: 25 nTPM
- breast: 21 nTPM
Single-cell type
- alveolar cells type 1: 653 nCPM
- astrocytes: 641 nCPM
- pituicytes/fscs: 543 nCPM
- transitional alveolar cells: 405 nCPM
- choroid plexus epithelial cells: 356 nCPM
- esophageal apical cells: 355 nCPM
Immune cell
- basophil: 0.6 nTPM
- neutrophil: 0.5 nTPM
- naive B-cell: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- choroid plexus: 57 nTPM
- midbrain: 44 nTPM
- thalamus: 43 nTPM
- basal ganglia: 41 nTPM
- amygdala: 39 nTPM
- cerebral cortex: 38 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.95
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.05
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular calcium ion homeostasis
- monoatomic ion transmembrane transport
- polyamine transmembrane transport
Molecular functions
- ATP binding
- ATP hydrolysis activity
- ATPase-coupled monoatomic cation transmembrane transporter activity
- metal ion binding
- P-type ion transporter activity
- polyamine transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- P-type ATPase
- Cation-transporting P-type ATPase, N-terminal
- P-type ATPase, subfamily V
- P-type ATPase, A domain superfamily
- P-type ATPase, phosphorylation site
- HAD superfamily
- P-type ATPase, transmembrane domain superfamily
- P-type ATPase, cytoplasmic domain N
- HAD-like superfamily
- P-type ATPase, haloacid dehalogenase domain
- P5B-type ATPase, N-terminal
- P5B-type ATPase
- P-type ATPase, A domain
- P-type ATPase actuator domain
- Cation transporter/ATPase, N-terminus
- P5-type ATPase cation transporter
- P-type ATPase, cytoplasmic domain N
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ATP13A4 as an antibody target. Whether an autoantibody or antibody against ATP13A4 could matter depends on whether native ATP13A4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATP13A4 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label ATP13A4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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