SPIB
Transcription factor Spi-B
Also known as: SPI-B, SPIB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q01892
- Gene
- SPIB
- Ensembl
- ENSG00000269404
- Chromosome
- 19
- Canonical length
- 262 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
The protein encoded by this gene is a transcriptional activator that binds to the PU-box (5'-GAGGAA-3') and acts as a lymphoid-specific enhancer. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
Canonical amino-acid sequenceUniProt
262 residues, UniProt reviewed canonical sequence.
>Q01892|SPIB
1 MLALEAAQLD GPHFSCLYPD GVFYDLDSCK HSSYPDSEGA PDSLWDWTVA PPVPATPYEA
61 FDPAAAAFSH PQAAQLCYEP PTYSPAGNLE LAPSLEAPGP GLPAYPTENF ASQTLVPPAY
121 APYPSPVLSE EEDLPLDSPA LEVSDSESDE ALVAGPEGKG SEAGTRKKLR LYQFLLGLLT
181 RGDMRECVWW VEPGAGVFQF SSKHKELLAR RWGQQKGNRK RMTYQKLARA LRNYAKTGEI
241 RKVKRKLTYQ FDSALLPAVR RALocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPIB 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)
- 0.58
- Highest tissue expression
- 93 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 93 nTPM
- lymph node: 82 nTPM
- appendix: 40 nTPM
- spleen: 27 nTPM
- small intestine: 25 nTPM
- colon: 21 nTPM
Single-cell type
- pdcs: 250 nCPM
- tuft cells: 231 nCPM
- colonocytes: 90 nCPM
- b-cells: 66 nCPM
- paneth cells: 31 nCPM
- enteric transient amplifying cells: 30 nCPM
Immune cell
- plasmacytoid DC: 574 nTPM
- memory B-cell: 309 nTPM
- naive B-cell: 262 nTPM
- total PBMC: 15 nTPM
- myeloid DC: 7 nTPM
- NK-cell: 3.9 nTPM
Brain region
- medulla oblongata: 5.9 nTPM
- white matter: 4.8 nTPM
- cerebellum: 4.5 nTPM
- cerebral cortex: 4 nTPM
- hypothalamus: 3.8 nTPM
- pons: 3.7 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)
- 0.39
- gnomAD pLI
- 0.91
- gnomAD missense Z
- 1.26
- DepMap mean gene effect
- -0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- immature B cell differentiation
- macrophage differentiation
- positive regulation of transcription by RNA polymerase II
- regulation of transcription by RNA polymerase II
Molecular functions
- DNA-binding transcription activator activity, RNA polymerase II-specific
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II cis-regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPIB 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 SPIB as an antibody target. Whether an autoantibody or antibody against SPIB could matter depends on whether native SPIB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPIB 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 SPIB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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