TAGLN3
Transgelin-3
Also known as: NP22, NP25, TAGL3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UI15
- Gene
- TAGLN3
- Ensembl
- ENSG00000144834
- Chromosome
- 3
- Canonical length
- 199 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable actin filament binding activity. Predicted to be involved in actin filament organization. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be active in actin cytoskeleton and synapse. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
199 residues, UniProt reviewed canonical sequence.
>Q9UI15|TAGLN3
1 MANRGPSYGL SREVQEKIEQ KYDADLENKL VDWIILQCAE DIEHPPPGRA HFQKWLMDGT
61 VLCKLINSLY PPGQEPIPKI SESKMAFKQM EQISQFLKAA ETYGVRTTDI FQTVDLWEGK
121 DMAAVQRTLM ALGSVAVTKD DGCYRGEPSW FHRKAQQNRR GFSEEQLRQG QNVIGLQMGS
181 NKGASQAGMT GYGMPRQIMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TAGLN3 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)
- 0.38
- Highest tissue expression
- 475 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 475 nTPM
- amygdala: 318 nTPM
- cerebellum: 290 nTPM
- basal ganglia: 283 nTPM
- hypothalamus: 264 nTPM
- hippocampal formation: 225 nTPM
Single-cell type
- retinal horizontal cells: 166 nCPM
- retinal amacrine cells: 101 nCPM
- other brain neurons: 95 nCPM
- bergmann glia: 94 nCPM
- brain excitatory neurons: 90 nCPM
- brain inhibitory neurons: 80 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 485 nTPM
- hypothalamus: 308 nTPM
- white matter: 294 nTPM
- pons: 281 nTPM
- basal ganglia: 276 nTPM
- medulla oblongata: 208 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)
- 0.72
- gnomAD pLI
- 0.18
- gnomAD missense Z
- 1.57
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin filament organization
- central nervous system development
- negative regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TAGLN3 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 TAGLN3 as an antibody target. Whether an autoantibody or antibody against TAGLN3 could matter depends on whether native TAGLN3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TAGLN3 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 TAGLN3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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