PRRT1
Proline-rich transmembrane protein 1
Also known as: C6orf31, DSPD1, IFITMD7, NG5, PRRT1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99946
- Gene
- PRRT1
- Ensembl
- ENSG00000204314
- Chromosome
- 6
- Canonical length
- 306 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
Enables identical protein binding activity. Predicted to be involved in several processes, including long-term synaptic depression; protein localization to cell surface; and regulation of AMPA receptor activity. Predicted to act upstream of or within several processes, including learning or memory; long-term synaptic potentiation; and synapse organization. Predicted to be located in plasma membrane and synaptic vesicle membrane. Predicted to be active in glutamatergic synapse and postsynaptic density membrane. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
306 residues, UniProt reviewed canonical sequence.
>Q99946|PRRT1
1 MSSEKSGLPD SVPHTSPPPY NAPQPPAEPP APPPQAAPSS HHHHHHHYHQ SGTATLPRLG
61 AGGLASSAAT AQRGPSSSAT LPRPPHHAPP GPAAGAPPPG CATLPRMPPD PYLQETRFEG
121 PLPPPPPAAA APPPPAPAQT AQAPGFVVPT HAGTVGTLPL GGYVAPGYPL QLQPCTAYVP
181 VYPVGTPYAG GTPGGTGVTS TLPPPPQGPG LALLEPRRPP HDYMPIAVLT TICCFWPTGI
241 IAIFKAVQVR TALARGDMVS AEIASREARN FSFISLAVGI AAMVLCTILT VVIIIAAQHH
301 ENYWDPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRRT1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.68
- Highest tissue expression
- 67 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 67 nTPM
- cerebral cortex: 51 nTPM
- basal ganglia: 29 nTPM
- hippocampal formation: 27 nTPM
- amygdala: 19 nTPM
- hypothalamus: 18 nTPM
Single-cell type
- brain excitatory neurons: 27 nCPM
- brain inhibitory neurons: 23 nCPM
- other brain neurons: 21 nCPM
- oligodendrocytes: 9.7 nCPM
- oligodendrocyte progenitor cells: 9.2 nCPM
- ependymal cells: 8.4 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- amygdala: 134 nTPM
- hippocampal formation: 133 nTPM
- cerebral cortex: 112 nTPM
- white matter: 63 nTPM
- thalamus: 37 nTPM
- basal ganglia: 35 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)
- 0.77
- gnomAD pLI
- 0.3
- gnomAD missense Z
- 3.03
- DepMap mean gene effect
- 0.07
- 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
- learning or memory
- long-term synaptic depression
- long-term synaptic potentiation
- protein localization to cell surface
- protein phosphorylation
- regulation of AMPA receptor activity
- synapse organization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PRRT1 as an antibody target. Whether an autoantibody or antibody against PRRT1 could matter depends on whether native PRRT1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRRT1 is annotated at the cell surface, where native PRRT1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label PRRT1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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