ZMYM5
Zinc finger MYM-type protein 5
Also known as: MYM, ZMYM5_HUMAN, ZNF198L1, ZNF237
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UJ78
- Gene
- ZMYM5
- Ensembl
- ENSG00000132950
- Chromosome
- 13
- Canonical length
- 669 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus
OverviewNCBI Gene
Predicted to enable zinc ion binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
669 residues, UniProt reviewed canonical sequence.
>Q9UJ78|ZMYM5
1 MEKCSVGGLE LTEQTPALLG NMAMATSLMD IGDSFGHPAC PLVSRSRNSP VEDDDDDDDV
61 VFIESIQPPS ISAPAIADQR NFIFASSKNE KPQGNYSVIP PSSRDLASQK GNISETIVID
121 DEEDIETNGG AEKKSSCFIE WGLPGTKNKT NDLDFSTSSL SRSKTKTGVR PFNPGRMNVA
181 GDLFQNGEFA THHSPDSWIS QSASFPSNQK QPGVDSLSPV ALLRKQNFQP TAQQQLTKPA
241 KITCANCKKP LQKGQTAYQR KGSAHLFCST TCLSSFSHKR TQNTRSIICK KDASTKKANV
301 ILPVESSKSF QEFYSTSCLS PCENNWNLKK GVFNKSRCTI CSKLAEIRHE VSVNNVTHKL
361 CSNHCFNKYR LANGLIMNCC EHCGEYMPSK STGNNILVIG GQQKRFCCQS CINEYKQMME
421 TKSKKLTASE NRKRNAFREE NEKQLYGSSN TLLKKIEGIP EKKEKTSQLQ LSVECGTDTL
481 LIQENVNLPP SSTSTIADTF QEQLEEKNFE DSIVPVVLSA DPGTWPRILN IKQRDTLVEN
541 VPPQVRNFNF PKDNTGRKFS ETYYTRILPN GEKTTRSWLL YSTSKDSVFC LYCKLFGEGK
601 NQLKNENGCK DWQHLSHILS KHEESEMHVN NSVKYSKLKS DLKKNKAIDA AEHRLYENEK
661 NDGVLLLYTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ZMYM5 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
- 0
- Mean surface accessibility (rSASA)
- 0.56
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- testis: 22 nTPM
- bone marrow: 12 nTPM
- lymph node: 9.6 nTPM
- thymus: 9.4 nTPM
- gallbladder: 8.6 nTPM
- retina: 8.4 nTPM
Single-cell type
- thymocytes: 160 nCPM
- early primary spermatocytes: 130 nCPM
- ocular epithelial cells: 105 nCPM
- neutrophils: 99 nCPM
- adrenal cortex cells: 95 nCPM
- choroid plexus epithelial cells: 91 nCPM
Immune cell
- basophil: 16 nTPM
- neutrophil: 11 nTPM
- memory B-cell: 9.9 nTPM
- memory CD4 T-cell: 9.9 nTPM
- MAIT T-cell: 9.3 nTPM
- T-reg: 8.9 nTPM
Brain region
- white matter: 13 nTPM
- choroid plexus: 11 nTPM
- medulla oblongata: 11 nTPM
- basal ganglia: 9.8 nTPM
- thalamus: 9.8 nTPM
- cerebellum: 9.7 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)
- 1.04
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.06
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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 ZMYM5 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 ZMYM5 as an antibody target. Whether an autoantibody or antibody against ZMYM5 could matter depends on whether native ZMYM5 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ZMYM5 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 ZMYM5 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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