ANKRD9
Ankyrin repeat domain-containing protein 9
Also known as: ANKR9_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96BM1
- Gene
- ANKRD9
- Ensembl
- ENSG00000156381
- Chromosome
- 14
- Canonical length
- 317 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables ubiquitin-like ligase-substrate adaptor activity. Involved in intracellular copper ion homeostasis; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Located in cytoplasmic vesicle and cytosol. Part of Cul5-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
317 residues, UniProt reviewed canonical sequence.
>Q96BM1|ANKRD9
1 MPWDARRPGG GADGGPEASG AARSRAQKQC RKSSFAFYQA VRDLLPVWLL EDMRASEAFH
61 WDERGRAAAY SPSEALLYAL VHDHQAYAHY LLATFPRRAL APPSAGFRCC AAPGPHVALA
121 VRYNRVGILR RILRTLRDFP AEERARVLDR RGCSRVEGGG TSLHVACELA RPECLFLLLG
181 HGASPGLRDG GGLTPLELLL RQLGRDAGAT PSAAGAPASA PGEPRQRRLL LLDLLALYTP
241 VGAAGSARQE LLGDRPRWQR LLGEDKFQWL AGLAPPSLFA RAMQVLVTAI SPGRFPEALD
301 ELPLPPFLQP LDLTGKGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ANKRD9 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)
- 0.3
- Highest tissue expression
- 149 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 149 nTPM
- heart muscle: 105 nTPM
- duodenum: 47 nTPM
- testis: 39 nTPM
- small intestine: 31 nTPM
- cerebral cortex: 29 nTPM
Single-cell type
- platelets: 241 nCPM
- early spermatids: 182 nCPM
- colonocytes: 160 nCPM
- enterocytes: 119 nCPM
- esophageal apical cells: 116 nCPM
- breast lactating cells: 90 nCPM
Immune cell
- non-classical monocyte: 0.4 nTPM
- basophil: 0.1 nTPM
- neutrophil: 0.1 nTPM
- NK-cell: 0.1 nTPM
- T-reg: 0.1 nTPM
- classical monocyte: 0 nTPM
Brain region
- cerebral cortex: 109 nTPM
- thalamus: 98 nTPM
- medulla oblongata: 97 nTPM
- amygdala: 81 nTPM
- spinal cord: 79 nTPM
- choroid plexus: 78 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)
- 1.19
- gnomAD pLI
- 0.29
- gnomAD missense Z
- 1.9
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- intracellular copper ion homeostasis
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein ubiquitination
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Ankyrin repeat
- Ankyrin repeat-containing domain superfamily
- E3 Ligase Complex Components and Neurotoxins
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ANKRD9 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 ANKRD9 as an antibody target. Whether an autoantibody or antibody against ANKRD9 could matter depends on whether native ANKRD9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ANKRD9 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 ANKRD9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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