ATXN7L3
Ataxin-7-like protein 3
Also known as: AT7L3_HUMAN, DKFZp761G2113
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q14CW9
- Gene
- ATXN7L3
- Ensembl
- ENSG00000087152
- Chromosome
- 17
- Canonical length
- 347 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles,Plasma membrane
OverviewNCBI Gene
Enables transcription coactivator activity. Involved in positive regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Located in nucleus. Part of DUBm complex and SAGA complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
347 residues, UniProt reviewed canonical sequence.
>Q14CW9|ATXN7L3
1 MKMEEMSLSG LDNSKLEAIA QEIYADLVED SCLGFCFEVH RAVKCGYFFL DDTDPDSMKD
61 FEIVDQPGLD IFGQVFNQWK SKECVCPNCS RSIAASRFAP HLEKCLGMGR NSSRIANRRI
121 ANSNNMNKSE SDQEDNDDIN DNDWSYGSEK KAKKRKSDKN PNSPRRSKSL KHKNGELSNS
181 DPFKYNNSTG ISYETLGPEE LRSLLTTQCG VISEHTKKMC TRSLRCPQHT DEQRRTVRIY
241 FLGPSAVLPE VESSLDNDSF DMTDSQALIS RLQWDGSSDL SPSDSGSSKT SENQGWGLGT
301 NSSESRKTKK KKSHLSLVGT ASGLGSNKKK KPKPPAPPTP SIYDDINLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ATXN7L3 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)
- 0.59
- Highest tissue expression
- 92 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 92 nTPM
- amygdala: 63 nTPM
- hippocampal formation: 54 nTPM
- bone marrow: 42 nTPM
- hypothalamus: 41 nTPM
- thymus: 39 nTPM
Single-cell type
- neutrophils: 59 nCPM
- late spermatids: 59 nCPM
- platelets: 55 nCPM
- tuft cells: 46 nCPM
- esophageal apical cells: 35 nCPM
- megakaryocytes: 31 nCPM
Immune cell
- neutrophil: 2.5 nTPM
- naive B-cell: 2.4 nTPM
- gdT-cell: 1.7 nTPM
- plasmacytoid DC: 1.6 nTPM
- eosinophil: 1.5 nTPM
- memory B-cell: 1.4 nTPM
Brain region
- cerebral cortex: 138 nTPM
- pons: 117 nTPM
- white matter: 102 nTPM
- amygdala: 98 nTPM
- basal ganglia: 98 nTPM
- thalamus: 94 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)
- 0.2
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.05
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
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 organization
- positive regulation of DNA-templated transcription
- regulation of DNA repair
- regulation of RNA splicing
- regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SCA7 domain
- SCA7, zinc-binding domain
- SAGA complex, Sgf11 subunit
- SAGA-associated factor 11
- Sgf11 (transcriptional regulation protein)
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ATXN7L3 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 ATXN7L3 as an antibody target. Whether an autoantibody or antibody against ATXN7L3 could matter depends on whether native ATXN7L3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ATXN7L3 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 ATXN7L3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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