TADA2A
Transcriptional adapter 2-alpha
Also known as: TAD2A_HUMAN
Protein identityUniProt · HPA
- UniProt accession
- O75478
- Gene
- TADA2A
- Canonical length
- 443 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
No narrative summary is available for TADA2A in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
443 residues, UniProt reviewed canonical sequence.
>O75478|TADA2A
1 MDRLGPFSND PSDKPPCRGC SSYLMEPYIK CAECGPPPFF LCLQCFTRGF EYKKHQSDHT
61 YEIMTSDFPV LDPSWTAQEE MALLEAVMDC GFGNWQDVAN QMCTKTKEEC EKHYMKHFIN
121 NPLFASTLLN LKQAEEAKTA DTAIPFHSTD DPPRPTFDSL LSRDMAGYMP ARADFIEEFD
181 NYAEWDLRDI DFVEDDSDIL HALKMAVVDI YHSRLKERQR RKKIIRDHGL INLRKFQLME
241 RRYPKEVQDL YETMRRFARI VGPVEHDKFI ESHALEFELR REIKRLQEYR TAGITNFCSA
301 RTYDHLKKTR EEERLKRTML SEVLQYIQDS SACQQWLRRQ ADIDSGLSPS IPMASNSGRR
361 SAPPLNLTGL PGTEKLNEKE KELCQMVRLV PGAYLEYKSA LLNECNKQGG LRLAQARALI
421 KIDVNKTRKI YDFLIREGYI TKGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TADA2A 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)
- 0.39
- Highest tissue expression
- 9.9 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 9.9 nTPM
- testis: 9.4 nTPM
- cerebral cortex: 7.4 nTPM
- hypothalamus: 6.2 nTPM
- midbrain: 6.2 nTPM
- basal ganglia: 6.1 nTPM
Single-cell type
- late spermatids: 52 nCPM
- renal collecting duct intercalated cells: 42 nCPM
- microglia: 42 nCPM
- renal connecting tubule cells: 39 nCPM
- renal collecting duct principal cells: 38 nCPM
- brain excitatory neurons: 35 nCPM
Immune cell
- plasmacytoid DC: 8.6 nTPM
- naive B-cell: 7.1 nTPM
- non-classical monocyte: 6 nTPM
- gdT-cell: 5.4 nTPM
- naive CD4 T-cell: 5.3 nTPM
- naive CD8 T-cell: 5.1 nTPM
Brain region
- cerebellum: 16 nTPM
- cerebral cortex: 14 nTPM
- white matter: 14 nTPM
- thalamus: 12 nTPM
- basal ganglia: 12 nTPM
- midbrain: 12 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)
- 0.85
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.46
- DepMap mean gene effect
- -0.56
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chromatin remodeling
- regulation of cell cycle
- regulation of cell division
- regulation of DNA-templated transcription
- regulation of embryonic development
- regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, ZZ-type
- SANT/Myb domain
- SWIRM domain
- Homedomain-like superfamily
- Transcriptional adaptor 2
- SANT domain
- Myb domain
- Winged helix-like DNA-binding domain superfamily
- ADA2-like, zinc finger, ZZ-type
- Zinc finger, ZZ-type superfamily
- Transcriptional adapter 2-alpha/beta-like domain
- Myb-like DNA-binding domain
- SWIRM domain
- Transcriptional adapter 2-alpha-like domain
- ADA2 ZZ-type zing finger
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TADA2A 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 TADA2A as an antibody target. Whether an autoantibody or antibody against TADA2A could matter depends on whether native TADA2A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TADA2A 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 TADA2A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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