Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8815
Gene name Gene Name - the full gene name approved by the HGNC.
Barrier to autointegration nuclear assembly factor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BANF1
Synonyms (NCBI Gene) Gene synonyms aliases
BAF, BCRP1, D14S1460, NGPS
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.1
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene was first identified by its ability to protect retroviruses from intramolecular integration and therefore promote intermolecular integration into the host cell genome. The protein forms a homodimer which localizes to both
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT815729 hsa-miR-1226 CLIP-seq
MIRT815730 hsa-miR-1255a CLIP-seq
MIRT815731 hsa-miR-1255b CLIP-seq
MIRT815732 hsa-miR-1289 CLIP-seq
MIRT815733 hsa-miR-150 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IDA 31796734
GO:0000793 Component Condensed chromosome IBA
GO:0000793 Component Condensed chromosome IDA 28841419
GO:0000793 Component Condensed chromosome IEA
GO:0003677 Function DNA binding IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603811 17397 ENSG00000175334
Protein
UniProt ID O75531
Protein name Barrier-to-autointegration factor (Breakpoint cluster region protein 1) [Cleaved into: Barrier-to-autointegration factor, N-terminally processed]
Protein function Non-specific DNA-binding protein that plays key roles in mitotic nuclear reassembly, chromatin organization, DNA damage response, gene expression and intrinsic immunity against foreign DNA (PubMed:10908652, PubMed:11792822, PubMed:12163470, PubM
PDB 1CI4 , 1QCK , 2BZF , 2EZX , 2EZY , 2EZZ , 2ODG , 6GHD , 6RPR , 6UNT , 6URE , 6URJ , 6URK , 6URL , 6URN , 6URR , 6URZ , 6US0 , 6US1 , 6US7 , 6USB , 6USD , 6USI , 7ABM , 7NDY , 7Z21 , 9J8M , 9J8N , 9J8O
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02961 BAF 1 88 Barrier to autointegration factor Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Expressed in colon, brain, heart, kidney, liver, lung, ovary, pancreas, placenta, prostate, skeletal muscle, small intestine, spleen and testis. Not detected in thymus and peripheral blood leukocytes. {ECO:0000269|Pub
Sequence
Sequence length 89
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Integration of provirus
2-LTR circle formation
Integration of viral DNA into host genomic DNA
Autointegration results in viral DNA circles
APOBEC3G mediated resistance to HIV-1 infection
Vpr-mediated nuclear import of PICs
Nuclear Envelope Breakdown
Initiation of Nuclear Envelope (NE) Reformation
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Nestor Guillermo Progeria Syndrome nestor-guillermo progeria syndrome rs387906871 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Aging Premature Associate 33660778, 36980188
Blood Coagulation Disorders Inherited Associate 21549337
Breast Neoplasms Stimulate 40664994
Carcinogenesis Associate 31392992
Carcinoma Hepatocellular Associate 29397868
Carcinoma Pancreatic Ductal Associate 37432996
Cataract Age Related Nuclear Associate 21549337
Coffin Siris syndrome Associate 33799280, 36352633
Developmental Disabilities Associate 33799280, 34753942, 34906496
Disease Associate 36980188