ZSWIM4
Zinc finger SWIM domain-containing protein 4
Also known as: FLJ12221, ZSWM4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H7M6
- Gene
- ZSWIM4
- Ensembl
- ENSG00000132003
- Chromosome
- 19
- Canonical length
- 989 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable zinc ion binding activity. Predicted to be part of Cul2-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
989 residues, UniProt reviewed canonical sequence.
>Q9H7M6|ZSWIM4
1 MEPPAAKRSR GCPAGPEERD AGAGAARGRG RPEALLDLSA KRVAESWAFE QVEERFSRVP
61 EPVQKRIVFW SFPRSEREIC MYSSLGYPPP EGEHDARVPF TRGLHLLQSG AVDRVLQVGF
121 HLSGNIREPG SPGEPERLYH VSISFDRCKI TSVSCGCDNR DLFYCAHVVA LSLYRIRHAH
181 QVELRLPISE TLSQMNRDQL QKFVQYLISA HHTEVLPTAQ RLADEILLLG SEINLVNGAP
241 DPTAGAGIED ANCWHLDEEQ IQEQVKQLLS NGGYYGASQQ LRSMFSKVRE MLRMRDSNGA
301 RMLILMTEQF LQDTRLALWR QQGAGMTDKC RQLWDELGAL WVCVVLSPHC KPEERAGWLQ
361 LLSRWDKLDV CPLEEGNYSF DGPSLQPTMA PAPELLQKGS TCITNTEGWV GHPLDPIGCL
421 CRALLEACRL EEETLTLYPD SGPEKRKVAY QHVPVPGSPG ESYLVLALEV ALLGLGQQRA
481 LPEGLYAQDK VVRNEEQLLA LLEEVELDER LVQVLRKQAG LLLEGGPFSG FGEVLFRESV
541 PMHTCARYLF TALLPHDPDL AYRLALRAMR LPILETAFPA GEPHPSPLDS IMSNRFPRWF
601 ILGHLETRQC ELASTMLTAA KGDPKWLHTV LGSIQQNIHS PALLFKLAQD ACKTATPVSA
661 PPDTTLLGIA LELGLQVMRM TLNVMTWRRR EMVRWLVSCA TEIGPQALMN IMQNWYSLFT
721 PVEAATIVAV TGTTHATLLR LQLDTSRREE LWACARTLAL QCAMKDPQNC ALPALTLCEK
781 NHSAFEAAYQ IVLDAAAGGL GHAHLFTVAR YMEHRGLPLR AYKLATLALA QLSIAFNQDS
841 HPAVNDVLWA CSLSHSLGRH ELSAIVPLII RSIHCAPMLS DILRRWTLSA PGLGPLGARR
901 AAKPLGADRA PLCQLLDAAV TAYITTSHSR LTHISPRHYG DFIEFLGKAR ETFLLAPDGH
961 LQFSQFLENL KQTYKGKKKL MLLVRERFGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZSWIM4 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 11 nTPM
Expression across tissuesHPA
Tissue
- esophagus: 11 nTPM
- salivary gland: 10 nTPM
- skin: 4.7 nTPM
- vagina: 4.7 nTPM
- cervix: 3.5 nTPM
- adrenal gland: 3.4 nTPM
Single-cell type
- papillary tip epithelial cells: 32 nCPM
- renal collecting duct principal cells: 21 nCPM
- loop of henle epithelial cells: 20 nCPM
- renal connecting tubule cells: 20 nCPM
- proximal tubule cells: 18 nCPM
- distal convoluted tubule cells: 14 nCPM
Immune cell
- neutrophil: 0.2 nTPM
- MAIT T-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebral cortex: 6.8 nTPM
- pons: 6.4 nTPM
- thalamus: 6.4 nTPM
- choroid plexus: 6.2 nTPM
- medulla oblongata: 6.1 nTPM
- midbrain: 5.9 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)
- 0.57
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.29
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ZSWIM4 as an antibody target. Whether an autoantibody or antibody against ZSWIM4 could matter depends on whether native ZSWIM4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZSWIM4 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 ZSWIM4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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