Gene Gene information from NCBI Gene database.
Entrez ID 79000
Gene name Aurora kinase A and ninein interacting protein
Gene symbol AUNIP
Synonyms (NCBI Gene)
AIBPC1orf135
Chromosome 1
Chromosome location 1p36.11
miRNA miRNA information provided by mirtarbase database.
3
miRTarBase ID miRNA Experiments Reference
MIRT016381 hsa-miR-193b-3p Microarray 20304954
MIRT030388 hsa-miR-24-3p Microarray 19748357
MIRT041773 hsa-miR-484 CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
20
GO ID Ontology Definition Evidence Reference
GO:0000724 Process Double-strand break repair via homologous recombination IDA 29042561
GO:0000922 Component Spindle pole IBA
GO:0000922 Component Spindle pole IDA 20596670
GO:0000922 Component Spindle pole IEA
GO:0003677 Function DNA binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620397 28363 ENSG00000127423
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H7T9
Protein name Aurora kinase A- and ninein-interacting protein (AIBp)
Protein function DNA-binding protein that accumulates at DNA double-strand breaks (DSBs) following DNA damage and promotes DNA resection and homologous recombination (PubMed:29042561). Serves as a sensor of DNA damage: binds DNA with a strong preference for DNA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15334 AIB 26 350 Aurora kinase A and ninein interacting protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in heart, skeletal muscles, placenta and testis.
Sequence
Sequence length 357
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
KIDNEY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Atherosclerosis Atherosclerosis BEFREE 30705153
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 31409573
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Parkinson disease Pubtator 37348876 Associate
★☆☆☆☆
Found in Text Mining only
Squamous cell carcinoma Carcinoma BEFREE 31409573
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Squamous cell carcinoma Pubtator 31409573 Associate
★☆☆☆☆
Found in Text Mining only