TSC22D4
TSC22 domain family protein 4
Also known as: T22D4_HUMAN, THG-1, TILZ2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y3Q8
- Gene
- TSC22D4
- Ensembl
- ENSG00000166925
- Chromosome
- 7
- Canonical length
- 395 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
TSC22D4 is a member of the TSC22 domain family of leucine zipper transcriptional regulators (see TSC22D3; MIM 300506) (Kester et al., 1999 [PubMed 10488076]; Fiorenza et al., 2001 [PubMed 11707329]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
395 residues, UniProt reviewed canonical sequence.
>Q9Y3Q8|TSC22D4
1 MSGGKKKSSF QITSVTTDYE GPGSPGASDP PTPQPPTGPP PRLPNGEPSP DPGGKGTPRN
61 GSPPPGAPSS RFRVVKLPHG LGEPYRRGRW TCVDVYERDL EPHSFGGLLE GIRGASGGAG
121 GRSLDSRLEL ASLGLGAPTP PSGLSQGPTS WLRPPPTSPG PQARSFTGGL GQLVVPSKAK
181 AEKPPLSASS PQQRPPEPET GESAGTSRAA TPLPSLRVEA EAGGSGARTP PLSRRKAVDM
241 RLRMELGAPE EMGQVPPLDS RPSSPALYFT HDASLVHKSP DPFGAVAAQK FSLAHSMLAI
301 SGHLDSDDDS GSGSLVGIDN KIEQAMDLVK SHLMFAVREE VEVLKEQIRE LAERNAALEQ
361 ENGLLRALAS PEQLAQLPSS GVPRLGPPAP NGPSVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TSC22D4 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)
- 0.69
- Highest tissue expression
- 851 nTPM
Expression across tissuesHPA
Tissue
- midbrain: 851 nTPM
- spinal cord: 767 nTPM
- basal ganglia: 692 nTPM
- amygdala: 632 nTPM
- hippocampal formation: 557 nTPM
- hypothalamus: 449 nTPM
Single-cell type
- müller glia: 441 nCPM
- esophageal apical cells: 389 nCPM
- retinal pigment epithelial cells: 290 nCPM
- bergmann glia: 246 nCPM
- oligodendrocytes: 239 nCPM
- schwann cells: 227 nCPM
Immune cell
- neutrophil: 56 nTPM
- eosinophil: 30 nTPM
- T-reg: 25 nTPM
- non-classical monocyte: 21 nTPM
- intermediate monocyte: 20 nTPM
- gdT-cell: 19 nTPM
Brain region
- basal ganglia: 858 nTPM
- midbrain: 785 nTPM
- white matter: 766 nTPM
- thalamus: 756 nTPM
- medulla oblongata: 712 nTPM
- cerebellum: 707 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)
- 0.3
- gnomAD pLI
- 0.96
- gnomAD missense Z
- 1
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- glucose homeostasis
- negative regulation of DNA-templated transcription
- negative regulation of transcription by RNA polymerase II
- neuron cellular homeostasis
- neuron projection extension
- response to osmotic stress
Cellular components
Protein domainsUniProt · Pfam · InterPro
- TSC22/Bun
- TSC22/Bun, conserved site
- TSC-22/dip/bun family
- TSC22 domain family protein 4
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TSC22D4 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 TSC22D4 as an antibody target. Whether an autoantibody or antibody against TSC22D4 could matter depends on whether native TSC22D4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TSC22D4 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 TSC22D4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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