APBB2
Amyloid beta precursor protein binding family B member 2
Also known as: APBB2_HUMAN, FE65L, FE65L1, MGC35575
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q92870
- Gene
- APBB2
- Ensembl
- ENSG00000163697
- Chromosome
- 4
- Canonical length
- 758 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
The protein encoded by this gene interacts with the cytoplasmic domains of amyloid beta (A4) precursor protein and amyloid beta (A4) precursor-like protein 2. This protein contains two phosphotyrosine binding (PTB) domains, which are thought to function in signal transduction. Polymorphisms in this gene have been associated with Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Canonical amino-acid sequenceUniProt
758 residues, UniProt reviewed canonical sequence.
>Q92870|APBB2
1 MSEVLPADSG VDTLAVFMAS SGTTDVTNRN SPATPPNTLN LRSSHNELLN AEIKHTETKN
61 STPPKCRKKY ALTNIQAAMG LSDPAAQPLL GNGSANIKLV KNGENQLRKA AEQGQQDPNK
121 NLSPTAVINI TSEKLEGKEP HPQDSSSCEI LPSQPRRTKS FLNYYADLET SARELEQNRG
181 NHHGTAEEKS QPVQGQASTI IGNGDLLLQK PNRPQSSPED GQVATVSSSP ETKKDHPKTG
241 AKTDCALHRI QNLAPSDEES SWTTLSQDSA SPSSPDETDI WSDHSFQTDP DLPPGWKRVS
301 DIAGTYYWHI PTGTTQWERP VSIPADLQGS RKGSLSSVTP SPTPENEKQP WSDFAVLNGG
361 KINSDIWKDL HAATVNPDPS LKEFEGATLR YASLKLRNAP HPDDDDSCSI NSDPEAKCFA
421 VRSLGWVEMA EEDLAPGKSS VAVNNCIRQL SYCKNDIRDT VGIWGEGKDM YLILENDMLS
481 LVDPMDRSVL HSQPIVSIRV WGVGRDNGRD FAYVARDKDT RILKCHVFRC DTPAKAIATS
541 LHEICSKIMA ERKNAKALAC SSLQERANVN LDVPLQVDFP TPKTELVQKF HVQYLGMLPV
601 DKPVGMDILN SAIENLMTSS NKEDWLSVNM NVADATVTVI SEKNEEEVLV ECRVRFLSFM
661 GVGKDVHTFA FIMDTGNQRF ECHVFWCEPN AGNVSEAVQA ACMLRYQKCL VARPPSQKVR
721 PPPPPADSVT RRVTTNVKRG VLSLIDTLKQ KRPVTEMPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against APBB2 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)
- 0.54
- Highest tissue expression
- 39 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 39 nTPM
- thyroid gland: 31 nTPM
- spinal cord: 30 nTPM
- cerebral cortex: 29 nTPM
- skeletal muscle: 27 nTPM
- blood vessel: 25 nTPM
Single-cell type
- podocytes: 1,784 nCPM
- distal convoluted tubule cells: 1,638 nCPM
- oligodendrocytes: 1,047 nCPM
- oligodendrocyte progenitor cells: 972 nCPM
- alveolar cells type 1: 927 nCPM
- adipocytes: 752 nCPM
Immune cell
- naive B-cell: 5.5 nTPM
- memory B-cell: 0.3 nTPM
- basophil: 0.2 nTPM
- classical monocyte: 0.2 nTPM
- myeloid DC: 0.2 nTPM
- total PBMC: 0.2 nTPM
Brain region
- white matter: 179 nTPM
- medulla oblongata: 124 nTPM
- basal ganglia: 120 nTPM
- midbrain: 116 nTPM
- pons: 115 nTPM
- cerebellum: 114 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)
- 0.44
- gnomAD pLI
- 0.07
- gnomAD missense Z
- 2.12
- DepMap mean gene effect
- 0.16
- DepMap dependency class
- none
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
- axon guidance
- extracellular matrix organization
- intracellular signal transduction
- maintenance of lens transparency
- negative regulation of apoptotic process
- negative regulation of transcription by RNA polymerase II
- neuron migration
- positive regulation of apoptotic process
- positive regulation of transcription by RNA polymerase II
- regulation of DNA-templated transcription
- smooth muscle contraction
- synapse organization
- negative regulation of cell cycle phase transition
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of APBB2 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 APBB2 as an antibody target. Whether an autoantibody or antibody against APBB2 could matter depends on whether native APBB2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
APBB2 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 APBB2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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