MINDY4
Probable ubiquitin carboxyl-terminal hydrolase MINDY-4
Also known as: C7orf67, FAM188B, FLJ22374, MINY4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q4G0A6
- Gene
- MINDY4
- Ensembl
- ENSG00000106125
- Chromosome
- 7
- Canonical length
- 757 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Vesicles,Cytosol
OverviewNCBI Gene
Predicted to enable K48-linked deubiquitinase activity. Predicted to be involved in protein K48-linked deubiquitination and proteolysis. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
757 residues, UniProt reviewed canonical sequence.
>Q4G0A6|MINDY4
1 MDSLFVEEVA ASLVREFLSR KGLKKTCVTM DQERPRSDLS INNRNDLRKV LHLEFLYKEN
61 KAKENPLKTS LELITRYFLD HFGNTANNFT QDTPIPALSV PKKNNKVPSR CSETTLVNIY
121 DLSDEDAGWR TSLSETSKAR HDNLDGDVLG NFVSSKRPPH KSKPMQTVPG ETPVLTSAWE
181 KIDKLHSEPS LDVKRMGENS RPKSGLIVRG MMSGPIASSP QDSFHRHYLR RSSPSSSSTQ
241 PQEESRKVPE LFVCTQQDIL ASSNSSPSRT SLGQLSELTV ERQKTTASSP PHLPSKRLPP
301 WDRARPRDPS EDTPAVDGST DTDRMPLKLY LPGGNSRMTQ ERLERAFKRQ GSQPAPVRKN
361 QLLPSDKVDG ELGALRLEDV EDELIREEVI LSPVPSVLKL QTASKPIDLS VAKEIKTLLF
421 GSSFCCFNEE WKLQSFSFSN TASLKYGIVQ NKGGPCGVLA AVQGCVLQKL LFEGDSKADC
481 AQGLQPSDAH RTRCLVLALA DIVWRAGGRE RAVVALASRT QQFSPTGKYK ADGVLETLTL
541 HSLTCYEDLV TFLQQSIHQF EVGPYGCILL TLSAILSRST ELIRQDFDVP TSHLIGAHGY
601 CTQELVNLLL TGKAVSNVFN DVVELDSGDG NITLLRGIAA RSDIGFLSLF EHYNMCQVGC
661 FLKTPRFPIW VVCSESHFSI LFSLQPGLLR DWRTERLFDL YYYDGLANQQ EQIRLTIDTT
721 QTISEDTDND LVPPLELCIR TKWKGASVNW NGSDPILLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MINDY4 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)
- 0.45
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 12 nTPM
- fallopian tube: 11 nTPM
- blood vessel: 10 nTPM
- lung: 9 nTPM
- testis: 8.6 nTPM
- ovary: 8.5 nTPM
Single-cell type
- ependymal cells: 19 nCPM
- endometrial ciliated cells: 7.8 nCPM
- gonadotrophs: 6.8 nCPM
- fallopian tube ciliated cells: 6.4 nCPM
- mesothelial cells: 4.5 nCPM
- thyrotrophs: 4.2 nCPM
Immune cell
- MAIT T-cell: 0.5 nTPM
- myeloid DC: 0.2 nTPM
- gdT-cell: 0.1 nTPM
- memory CD4 T-cell: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
- T-reg: 0.1 nTPM
Brain region
- choroid plexus: 28 nTPM
- midbrain: 15 nTPM
- cerebral cortex: 13 nTPM
- basal ganglia: 12 nTPM
- medulla oblongata: 11 nTPM
- hypothalamus: 9.9 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)
- 1.13
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Protein domainsUniProt · Pfam · InterPro
- Deubiquitinating enzyme MINDY-3/4, conserved domain
- Deubiquitinating enzyme MINDY-3/4
- Deubiquitinating enzyme MINDY-3/4, conserved domain
- MINDY4, N-terminal dimerisation domain
- MINDY4, N-terminal dimerisation domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MINDY4 as an antibody target. Whether an autoantibody or antibody against MINDY4 could matter depends on whether native MINDY4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MINDY4 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 MINDY4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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