PNISR
Arginine/serine-rich protein PNISR
Also known as: bA98I9.2, C6orf111, DKFZp564B0769, FLJ14752, PNISR_HUMAN, SFRS18, SRrp130
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TF01
- Gene
- PNISR
- Ensembl
- ENSG00000132424
- Chromosome
- 6
- Canonical length
- 805 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles,Plasma membrane,Cytosol
OverviewNCBI Gene
Enables RNA binding activity. Located in cytosol; nuclear speck; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
805 residues, UniProt reviewed canonical sequence.
>Q8TF01|PNISR
1 MWDQGGQPWQ QWPLNQQQWM QSFQHQQDPS QIDWAALAQA WIAQREASGQ QSMVEQPPGM
61 MPNGQDMSTM ESGPNNHGNF QGDSNFNRMW QPEWGMHQQP PHPPPDQPWM PPTPGPMDIV
121 PPSEDSNSQD SGEFAPDNRH IFNQNNHNFG GPPDNFAVGP VNQFDYQHGA AFGPPQGGFH
181 PPYWQPGPPG PPAPPQNRRE RPSSFRDRQR SPIALPVKQE PPQIDAVKRR TLPAWIREGL
241 EKMEREKQKK LEKERMEQQR SQLSKKEKKA TEDAEGGDGP RLPQRSKFDS DEEEEDTENV
301 EAASSGKVTR SPSPVPQEEH SDPEMTEEEK EYQMMLLTKM LLTEILLDVT DEEIYYVAKD
361 AHRKATKAPA KQLAQSSALA SLTGLGGLGG YGSGDSEDER SDRGSESSDT DDEELRHRIR
421 QKQEAFWRKE KEQQLLHDKQ MEEEKQQTER VTKEMNEFIH KEQNSLSLLE AREADGDVVN
481 EKKRTPNETT SVLEPKKEHK EKEKQGRSRS GSSSSGSSSS NSRTSSTSST VSSSSYSSSS
541 GSSRTSSRSS SPKRKKRHSR SRSPTIKARR SRSRSYSRRI KIESNRARVK IRDRRRSNRN
601 SIERERRRNR SPSRERRRSR SRSRDRRTNR ASRSRSRDRR KIDDQRGNLS GNSHKHKGEA
661 KEQERKKERS RSIDKDRKKK DKEREREQDK RKEKQKREEK DFKFSSQDDR LKRKRESERT
721 FSRSGSISVK IIRHDSRQDS KKSTTKDSKK HSGSDSSGRS SSESPGSSKE KKAKKPKHSR
781 SRSVEKSQRS GKKASRKHKS KSRSRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PNISR 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)
- 0.65
- Highest tissue expression
- 128 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 128 nTPM
- ovary: 103 nTPM
- bone marrow: 101 nTPM
- thyroid gland: 97 nTPM
- colon: 97 nTPM
- retina: 95 nTPM
Single-cell type
- leydig cells: 867 nCPM
- pituitary stem cells: 586 nCPM
- pituicytes/fscs: 581 nCPM
- sertoli cells: 579 nCPM
- somatotrophs: 578 nCPM
- epididymal principal cells: 574 nCPM
Immune cell
- neutrophil: 30 nTPM
- naive B-cell: 26 nTPM
- NK-cell: 24 nTPM
- plasmacytoid DC: 20 nTPM
- memory B-cell: 19 nTPM
- naive CD4 T-cell: 18 nTPM
Brain region
- cerebellum: 118 nTPM
- choroid plexus: 98 nTPM
- cerebral cortex: 83 nTPM
- white matter: 79 nTPM
- medulla oblongata: 77 nTPM
- thalamus: 75 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)
- 0.18
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.61
- DepMap mean gene effect
- -0.46
- DepMap dependency class
- selective
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- PNN-interacting serine/arginine-rich protein
- Arginine/serine-rich protein PNISR
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PNISR 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 PNISR as an antibody target. Whether an autoantibody or antibody against PNISR could matter depends on whether native PNISR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PNISR 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 PNISR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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