AUNIP
Aurora kinase A- and ninein-interacting protein
Also known as: AIBp, AUNIP_HUMAN, C1orf135, MGC2603
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H7T9
- Gene
- AUNIP
- Ensembl
- ENSG00000127423
- Chromosome
- 1
- Canonical length
- 357 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Centrosome
OverviewNCBI Gene
Enables damaged DNA binding activity. Involved in double-strand break repair via homologous recombination; negative regulation of double-strand break repair via nonhomologous end joining; and spindle organization. Located in centrosome; site of DNA damage; and spindle pole. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
357 residues, UniProt reviewed canonical sequence.
>Q9H7T9|AUNIP
1 MRRTGPEEEA CGVWLDAAAL KRRKVQTHLI KPGTKMLTLL PGERKANIYF TQRRAPSTGI
61 HQRSIASFFT LQPGKTNGSD QKSVSSHTES QINKESKKNA TQLDHLIPGL AHDCMASPLA
121 TSTTADIQEA GLSPQSLQTS GHHRMKTPFS TELSLLQPDT PDCAGDSHTP LAFSFTEDLE
181 SSCLLDRKEE KGDSARKWEW LHESKKNYQS MEKHTKLPGD KCCQPLGKTK LERKVSAKEN
241 RQAPVLLQTY RESWNGENIE SVKQSRSPVS VFSWDNEKND KDSWSQLFTE DSQGQRVIAH
301 NTRAPFQDVT NNWNWDLGPF PNSPWAQCQE DGPTQNLKPD LLFTQDSEGN QVIRHQFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against AUNIP 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)
- 0.7
- Highest tissue expression
- 15 nTPM
Expression across tissuesHPA
Tissue
- testis: 15 nTPM
- bone marrow: 5.9 nTPM
- placenta: 1.6 nTPM
- tonsil: 1.6 nTPM
- esophagus: 1.3 nTPM
- cerebral cortex: 1.2 nTPM
Single-cell type
- late spermatids: 186 nCPM
- early primary spermatocytes: 81 nCPM
- oocytes: 78 nCPM
- cardiomyocytes: 75 nCPM
- early spermatids: 67 nCPM
- epicardial cells: 48 nCPM
Immune cell
- basophil: 1.5 nTPM
- intermediate monocyte: 1 nTPM
- T-reg: 0.8 nTPM
- classical monocyte: 0.7 nTPM
- myeloid DC: 0.6 nTPM
- non-classical monocyte: 0.6 nTPM
Brain region
- cerebellum: 4 nTPM
- cerebral cortex: 4 nTPM
- amygdala: 3.3 nTPM
- white matter: 3.3 nTPM
- pons: 3.1 nTPM
- basal ganglia: 2.9 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)
- 1.58
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.3
- DepMap mean gene effect
- -0.02
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- double-strand break repair via homologous recombination
- negative regulation of double-strand break repair via nonhomologous end joining
- spindle organization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Aurora kinase A- and ninein interacting protein
- Aurora kinase A and ninein interacting protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of AUNIP 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 AUNIP as an antibody target. Whether an autoantibody or antibody against AUNIP could matter depends on whether native AUNIP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AUNIP 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 AUNIP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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