Gene Gene information from NCBI Gene database.
Entrez ID 322
Gene name Amyloid beta precursor protein binding family B member 1
Gene symbol APBB1
Synonyms (NCBI Gene)
FE65MGC:9072RIR
Chromosome 11
Chromosome location 11p15.4
Summary The protein encoded by this gene is a member of the Fe65 protein family. It is an adaptor protein localized in the nucleus. It interacts with the Alzheimer`s disease amyloid precursor protein (APP), transcription factor CP2/LSF/LBP1 and the low-density li
miRNA miRNA information provided by mirtarbase database.
78
miRTarBase ID miRNA Experiments Reference
MIRT017493 hsa-miR-335-5p Microarray 18185580
MIRT019356 hsa-miR-148b-3p Microarray 17612493
MIRT043469 hsa-miR-331-3p CLASH 23622248
MIRT1932634 hsa-miR-1909 CLIP-seq
MIRT1932635 hsa-miR-4641 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
46
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IGI 21803450
GO:0001540 Function Amyloid-beta binding IBA
GO:0001540 Function Amyloid-beta binding IEA
GO:0003682 Function Chromatin binding IDA 19343227
GO:0003713 Function Transcription coactivator activity TAS 12153398
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602709 581 ENSG00000166313
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O00213
Protein name Amyloid beta precursor protein binding family B member 1 (Amyloid-beta A4 precursor protein-binding family B member 1) (Protein Fe65)
Protein function Transcription coregulator that can have both coactivator and corepressor functions (PubMed:15031292, PubMed:18468999, PubMed:18922798, PubMed:25342469, PubMed:33938178). Adapter protein that forms a transcriptionally active complex with the gamm
PDB 2E45 , 2HO2 , 2IDH , 2OEI , 3D8D , 3D8E , 3D8F , 3DXC , 3DXD , 3DXE , 5NQH
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00397 WW 255 283 WW domain Domain
PF00640 PID 370 509 Phosphotyrosine interaction domain (PTB/PID) Domain
PF00640 PID 543 664 Phosphotyrosine interaction domain (PTB/PID) Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in brain; strongly reduced in post-mortem elderly subjects with Alzheimer disease. {ECO:0000269|PubMed:19343227}.; TISSUE SPECIFICITY: [Isoform 4]: Expressed preferentially in the brain. {ECO:0000269|PubMed:21824145}.
Sequence
MSVPSSLSQSAINANSHGGPALSLPLPLHAAHNQLLNAKLQATAVGPKDLRSAMGEGGGP
EPGPANAKWLKEGQNQLRRAATAHRDQNRNVTLTLAEEASQEPEMAPLGPKGLIHLYSEL
ELSAHNAANRGLRGPGLIISTQEQGPDEGEEKAAGEAEEEEEDDDDEEEEEDLSSPPGLP
EPLESVEAPPRPQALTDGPREHSKSASLLFGMRNSAASDEDSSWATLSQGSPSYGSPEDT
DSFWNPNAFETDSDLPAGWMRVQDTSGTYYWHIPTGTTQWEPPGRASPSQGSSPQEESQL
TWTGFAHGEGFEDGEFWKDEPSDEAPMELGLKEPEEGTLTFPAQSLSPEPLPQEEEKLPP
RNTNPGIKCFAVRSLGWVEMTEEELAPGRSSVAVNNCIRQLSYHKNNLHDPMSGGWGEGK
DLLLQLEDETLKLVEPQSQALLHAQPIISIRVWGVGRDSGRERDFAYVARDKLTQMLKCH
VFRCEAPAKNIATSLHEICSKIMAERRNA
RCLVNGLSLDHSKLVDVPFQVEFPAPKNELV
QKFQVYYLGNVPVAKPVGVDVINGALESVLSSSSREQWTPSHVSVAPATLTILHQQTEAV
LGECRVRFLSFLAVGRDVHTFAFIMAAGPASFCCHMFWCEPNAASLSEAVQAACMLRYQK
CLDA
RSQASTSCLPAPPAESVARRVGWTVRRGVQSLWGSLKPKRLGAHTP
Sequence length 710
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Alzheimer disease   Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
ALZHEIMERS DISEASE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
APBB1-related disorder Uncertain significance; Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NIEMANN-PICK DISEASE, TYPE A Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NIEMANN-PICK DISEASE, TYPE B Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 12951770, 17170108, 18550529, 18777128, 21415543, 23167255, 26166158, 28323844, 32751526
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease Stimulate 22952038
★☆☆☆☆
Found in Text Mining only
Autism Spectrum Disorder Associate 33562221
★☆☆☆☆
Found in Text Mining only
Autistic Disorder Associate 24853428
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 24619425
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Inhibit 26166158
★☆☆☆☆
Found in Text Mining only
DNA Virus Infections Associate 27176072
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Associate 28323844
★☆☆☆☆
Found in Text Mining only
Neurodegenerative Diseases Associate 18777128, 24619425
★☆☆☆☆
Found in Text Mining only
Parkinson Disease Associate 18777128
★☆☆☆☆
Found in Text Mining only