KANSL2
KAT8 regulatory NSL complex subunit 2
Also known as: C12orf41, FLJ20436, KANL2_HUMAN, NSL2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H9L4
- Gene
- KANSL2
- Ensembl
- ENSG00000139620
- Chromosome
- 12
- Canonical length
- 492 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
Predicted to be involved in positive regulation of DNA-templated transcription. Located in several cellular components, including actin cytoskeleton; cytosol; and nucleoplasm. Part of NSL complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
492 residues, UniProt reviewed canonical sequence.
>Q9H9L4|KANSL2
1 MNRIRIHVLP TNRGRITPVP RSQEPLSCAF THRPCSHPRL EGQEFCIKHI LEDKNAPFKQ
61 CSYISTKNGK RCPNAAPKPE KKDGVSFCAE HVRRNALALH AQMKKTNPGP VGETLLCQLS
121 SYAKTELGSQ TPESSRSEAS RILDEDSWSD GEQEPITVDQ TWRGDPDSEA DSIDSDQEDP
181 LKHAGVYTAE EVALIMREKL IRLQSLYIDQ FKRLQHLLKE KKRRYLHNRK VEHEALGSSL
241 LTGPEGLLAK ERENLKRLKC LRRYRQRYGV EALLHRQLKE RRMLATDGAA QQAHTTRSSQ
301 RCLAFVDDVR CSNQSLPMTR HCLTHICQDT NQVLFKCCQG SEEVPCNKPV PVSLSEDPCC
361 PLHFQLPPQM YKPEQVLSVP DDLEAGPMDL YLSAAELQPT ESLPLEFSDD LDVVGDGMQC
421 PPSPLLFDPS LTLEDHLVKE IAEDPVDILG QMQMAGDGCR SQGSRNSEKA SAPLSQSGLA
481 TANGKPEPTS ISLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KANSL2 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)
- 0.56
- Highest tissue expression
- 40 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 40 nTPM
- skeletal muscle: 34 nTPM
- tongue: 22 nTPM
- cerebellum: 13 nTPM
- thymus: 13 nTPM
- lymph node: 13 nTPM
Single-cell type
- neutrophil progenitors: 70 nCPM
- myonuclei: 67 nCPM
- innate lymphoid cells: 65 nCPM
- early primary spermatocytes: 60 nCPM
- nk-cells: 54 nCPM
- t-cells: 52 nCPM
Immune cell
- basophil: 36 nTPM
- T-reg: 32 nTPM
- naive CD4 T-cell: 28 nTPM
- memory B-cell: 28 nTPM
- naive CD8 T-cell: 27 nTPM
- memory CD8 T-cell: 26 nTPM
Brain region
- cerebellum: 14 nTPM
- white matter: 14 nTPM
- choroid plexus: 11 nTPM
- cerebral cortex: 11 nTPM
- medulla oblongata: 11 nTPM
- basal ganglia: 10 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)
- 0.37
- gnomAD pLI
- 0.88
- gnomAD missense Z
- 1.49
- DepMap mean gene effect
- -1.1
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
- KANL2-like, probable zinc-finger domain
- KANL2-like, probable zinc-finger domain
- KAT8 regulatory NSL complex subunit 2
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KANSL2 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 KANSL2 as an antibody target. Whether an autoantibody or antibody against KANSL2 could matter depends on whether native KANSL2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KANSL2 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 KANSL2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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