BCAS2
Pre-mRNA-splicing factor SPF27
Also known as: DAM1, Snt309, SPF27, SPF27_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75934
- Gene
- BCAS2
- Ensembl
- ENSG00000116752
- Chromosome
- 1
- Canonical length
- 225 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles,Centrosome
- Quaternary structure
- Homotetramer
OverviewNCBI Gene
Involved in mRNA splicing, via spliceosome. Located in DNA replication factor A complex; centrosome; and nuclear speck. Part of Prp19 complex and U2-type catalytic step 2 spliceosome. Implicated in breast cancer. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
225 residues, UniProt reviewed canonical sequence.
>O75934|BCAS2
1 MAGTGLVAGE VVVDALPYFD QGYEAPGVRE AAAALVEEET RRYRPTKNYL SYLTAPDYSA
61 FETDIMRNEF ERLAARQPIE LLSMKRYELP APSSGQKNDI TAWQECVNNS MAQLEHQAVR
121 IENLELMSQH GCNAWKVYNE NLVHMIEHAQ KELQKLRKHI QDLNWQRKNM QLTAGSKLRE
181 MESNWVSLVS KNYEIERTIV QLENEIYQIK QQHGEANKEN IRQDFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BCAS2 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)
- 0.49
- Highest tissue expression
- 72 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 72 nTPM
- skeletal muscle: 53 nTPM
- liver: 48 nTPM
- hypothalamus: 47 nTPM
- cerebral cortex: 47 nTPM
- epididymis: 47 nTPM
Single-cell type
- oocytes: 410 nCPM
- ocular epithelial cells: 254 nCPM
- esophageal basal cells: 243 nCPM
- ovarian stromal cells: 243 nCPM
- endometrial glandular cells: 235 nCPM
- esophageal suprabasal cells: 231 nCPM
Immune cell
- MAIT T-cell: 79 nTPM
- T-reg: 78 nTPM
- NK-cell: 75 nTPM
- naive CD4 T-cell: 74 nTPM
- total PBMC: 73 nTPM
- naive CD8 T-cell: 72 nTPM
Brain region
- hypothalamus: 43 nTPM
- cerebral cortex: 42 nTPM
- pons: 42 nTPM
- midbrain: 41 nTPM
- white matter: 39 nTPM
- cerebellum: 38 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)
- 1.33
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.52
- DepMap mean gene effect
- -1.33
- DepMap dependency class
- pan
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
- alternative mRNA splicing, via spliceosome
- mRNA splicing, via spliceosome
- oocyte development
- ovarian follicle development
- protein catabolic process
- RNA splicing
- RNA splicing, via transesterification reactions
- spindle assembly
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Pre-mRNA-splicing factor SPF27
- Breast carcinoma amplified sequence 2 (BCAS2)
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BCAS2 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 BCAS2 as an antibody target. Whether an autoantibody or antibody against BCAS2 could matter depends on whether native BCAS2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BCAS2 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 BCAS2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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