PRRC1
Protein PRRC1
Also known as: FLJ32875, PRRC1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96M27
- Gene
- PRRC1
- Ensembl
- ENSG00000164244
- Chromosome
- 5
- Canonical length
- 445 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Vesicles
OverviewNCBI Gene
Predicted to enable protein kinase A regulatory subunit binding activity. Predicted to be involved in epithelial structure maintenance. Predicted to be located in Golgi apparatus. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
445 residues, UniProt reviewed canonical sequence.
>Q96M27|PRRC1
1 MMEESGIETT PPGTPPPNPA GLAATAMSST PVPLAATSSF SSPNVSSMES FPPLAYSTPQ
61 PPLPPVRPSA PLPFVPPPAV PSVPPLVTSM PPPVSPSTAA AFGNPPVSHF PPSTSAPNTL
121 LPAPPSGPPI SGFSVGSTYD ITRGHAGRAP QTPLMPSFSA PSGTGLLPTP ITQQASLTSL
181 AQGTGTTSAI TFPEEQEDPR ITRGQDEASA GGIWGFIKGV AGNPMVKSVL DKTKHSVESM
241 ITTLDPGMAP YIKSGGELDI VVTSNKEVKV AAVRDAFQEV FGLAVVVGEA GQSNIAPQPV
301 GYAAGLKGAQ ERIDSLRRTG VIHEKQTAVS VENFIAELLP DKWFDIGCLV VEDPVHGIHL
361 ETFTQATPVP LEFVQQAQSL TPQDYNLRWS GLLVTVGEVL EKSLLNVSRT DWHMAFTGMS
421 RRQMIYSAAR AIAGMYKQRL PPRTVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRRC1 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)
- 0.52
- Highest tissue expression
- 30 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 30 nTPM
- parathyroid gland: 29 nTPM
- cervix: 26 nTPM
- rectum: 26 nTPM
- placenta: 25 nTPM
- liver: 25 nTPM
Single-cell type
- lactotrophs: 99 nCPM
- somatotrophs: 98 nCPM
- corticotrophs: 75 nCPM
- extravillous trophoblasts: 69 nCPM
- pancreatic acinar cells: 69 nCPM
- gonadotrophs: 64 nCPM
Immune cell
- MAIT T-cell: 23 nTPM
- gdT-cell: 19 nTPM
- basophil: 19 nTPM
- naive CD4 T-cell: 17 nTPM
- memory CD8 T-cell: 16 nTPM
- myeloid DC: 16 nTPM
Brain region
- choroid plexus: 25 nTPM
- white matter: 19 nTPM
- medulla oblongata: 16 nTPM
- cerebellum: 16 nTPM
- midbrain: 15 nTPM
- basal ganglia: 15 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)
- 1.48
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.02
- DepMap mean gene effect
- 0.02
- 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
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Inosine triphosphate pyrophosphatase-like
- Non-canonical purine NTP phosphatase/PRRC1
- Protein PRRC1
- Protein of unknown function DUF84
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PRRC1 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 PRRC1 as an antibody target. Whether an autoantibody or antibody against PRRC1 could matter depends on whether native PRRC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRRC1 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 PRRC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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