ATP1B4
Protein ATP1B4
Also known as: AT1B4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UN42
- Gene
- ATP1B4
- Ensembl
- ENSG00000101892
- Chromosome
- X
- Canonical length
- 357 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
This gene has been found in all vertebrate genomes sequenced to date. However, this gene has undergone a change in function in placental mammals compared to other species. Specifically, in fish, avian, and amphibian species, this gene encodes plasma membrane-bound beta-subunits of Na,K-ATPase. In placental mammals, the encoded protein interacts with the nuclear transcriptional coregulator SKIP and may be involved in the regulation of TGF-beta signaling. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]
Canonical amino-acid sequenceUniProt
357 residues, UniProt reviewed canonical sequence.
>Q9UN42|ATP1B4
1 MRRQLRSRRA PSFPYSYRYR LDDPDEANQN YLADEEEEAE EEARVTVVPK SEEEEEEEEK
61 EEEEEEEKEE EEGQGQPTGN AWWQKLQIMS EYLWDPERRM FLARTGQSWS LILLIYFFFY
121 ASLAAVITLC MYTLFLTISP YIPTFTERVK PPGVMIRPFA HSLNFNFNVS EPDTWQHYVI
181 SLNGFLQGYN DSLQEEMNVD CPPGQYFIQD GNEDEDKKAC QFKRSFLKNC SGLEDPTFGY
241 STGQPCILLK MNRIVGFRPE LGDPVKVSCK VQRGDENDIR SISYYPESAS FDLRYYPYYG
301 KLTHVNYTSP LVAMHFTDVV KNQAVPVQCQ LKGKGVINDV INDRFVGRVI FTLNIETLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATP1B4 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.37
- Highest tissue expression
- 52 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 52 nTPM
- tongue: 20 nTPM
- heart muscle: 1.2 nTPM
- prostate: 1.2 nTPM
- esophagus: 0.6 nTPM
- salivary gland: 0.3 nTPM
Single-cell type
- myonuclei: 242 nCPM
- thymic myoid cells: 31 nCPM
- fibro-adipogenic progenitors: 2 nCPM
- adipocytes: 1.5 nCPM
- ependymal cells: 0.8 nCPM
- pituitary stem cells: 0.7 nCPM
Immune cell
- basophil: 0.1 nTPM
- neutrophil: 0.1 nTPM
- total PBMC: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebellum: 1 nTPM
- hippocampal formation: 1 nTPM
- white matter: 1 nTPM
- cerebral cortex: 0.9 nTPM
- amygdala: 0.8 nTPM
- hypothalamus: 0.8 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)
- 0.92
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.22
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ATP1B4 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ATP1B4 as an antibody target. Whether an autoantibody or antibody against ATP1B4 could matter depends on whether native ATP1B4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATP1B4 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 ATP1B4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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