ANKS4B
Ankyrin repeat and SAM domain-containing protein 4B
Also known as: ANS4B_HUMAN, FLJ38819, HARP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N8V4
- Gene
- ANKS4B
- Ensembl
- ENSG00000175311
- Chromosome
- 16
- Canonical length
- 417 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Involved in brush border assembly; protein localization to microvillus; and protein-containing complex assembly. Located in brush border and microvillus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
417 residues, UniProt reviewed canonical sequence.
>Q8N8V4|ANKS4B
1 MSTRYHQAAS DSYLELLKEA TKRDLNLSDE DGMTPTLLAA YHGNLEALEI ICSRGGDPDR
61 CDIWGNTPLH FAASNGHAHC VSFLVNFGAN IFALDNDLQT PLDAAASREQ NECVALLDKA
121 ATAQNIMNPK KVTRLKEQAQ KNARRQIKEC ERLQEKHQNK MAHTYSKEES GTLSSSKGTF
181 SRSSPSNASA PGTFGSLSKG IKDTFKIKFK KNKDTAEQVG KEGRSGQRNV MEVFREEEED
241 SFSGDFKEKL QLSAEEDGSV HHESILNRPG LGSIVFRRNR ISSPEDISDS KREFGFKLPS
301 ELLQRQGASE ADEGAADEEG EENGLKDDLP WDDDEVEWEE DVVDATPLEV FLLSQHLEEF
361 LPIFKREQID LEALLLCSDE DLQSIQMQLG PRKKVLNAIN RRKQVLQQPG QLVDTSLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ANKS4B 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)
- 0.49
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- liver: 13 nTPM
- small intestine: 12 nTPM
- duodenum: 8.4 nTPM
- colon: 8.3 nTPM
- rectum: 6.7 nTPM
- kidney: 5.5 nTPM
Single-cell type
- proximal tubule cells: 41 nCPM
- brain excitatory neurons: 4.3 nCPM
- brain inhibitory neurons: 1.9 nCPM
- podocytes: 1.3 nCPM
- distal convoluted tubule cells: 1.2 nCPM
- papillary tip epithelial cells: 1.1 nCPM
Immune cell
- basophil: 0.2 nTPM
- neutrophil: 0.2 nTPM
- NK-cell: 0.1 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebellum: 5.8 nTPM
- basal ganglia: 2.1 nTPM
- cerebral cortex: 2 nTPM
- hippocampal formation: 1.8 nTPM
- white matter: 1.8 nTPM
- pons: 1.7 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)
- 1.24
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.9
- DepMap mean gene effect
- 0.21
- 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
- brush border assembly
- cell differentiation
- protein localization to microvillus
- protein-containing complex assembly
- response to endoplasmic reticulum stress
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ANKS4B 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 ANKS4B as an antibody target. Whether an autoantibody or antibody against ANKS4B could matter depends on whether native ANKS4B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ANKS4B 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 ANKS4B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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