NRARP
Notch-regulated ankyrin repeat-containing protein
Also known as: MGC61598, NRARP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z6K4
- Gene
- NRARP
- Ensembl
- ENSG00000198435
- Chromosome
- 9
- Canonical length
- 114 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Involved in Notch signaling pathway. Acts upstream of or within negative regulation of Notch signaling pathway and positive regulation of canonical Wnt signaling pathway. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
114 residues, UniProt reviewed canonical sequence.
>Q7Z6K4|NRARP
1 MSQAELSTCS APQTQRIFQE AVRKGNTQEL QSLLQNMTNC EFNVNSFGPE GQTALHQSVI
61 DGNLELVKLL VKFGADIRLA NRDGWSALHI AAFGGHQDIV LYLITKAKYA ASGRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NRARP 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 45 nTPM
Expression across tissuesHPA
Tissue
- colon: 45 nTPM
- skin: 34 nTPM
- esophagus: 31 nTPM
- rectum: 29 nTPM
- duodenum: 21 nTPM
- heart muscle: 18 nTPM
Single-cell type
- suprabasal keratinocytes: 381 nCPM
- ocular epithelial cells: 178 nCPM
- prostatic club cells: 178 nCPM
- prostatic hillock cells: 157 nCPM
- colonocytes: 152 nCPM
- basal keratinocytes: 144 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
- hypothalamus: 26 nTPM
- midbrain: 21 nTPM
- thalamus: 19 nTPM
- medulla oblongata: 19 nTPM
- pons: 17 nTPM
- spinal cord: 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)
- 1.5
- gnomAD pLI
- 0.21
- gnomAD missense Z
- 2.33
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
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
- blood vessel endothelial cell proliferation involved in sprouting angiogenesis
- branching involved in blood vessel morphogenesis
- negative regulation of Notch signaling pathway
- negative regulation of T cell differentiation
- negative regulation of transcription by RNA polymerase II
- Notch signaling pathway
- positive regulation of canonical Wnt signaling pathway
- positive regulation of vascular endothelial cell proliferation
- somite rostral/caudal axis specification
- T cell differentiation
- vascular endothelial cell proliferation
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NRARP 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 NRARP as an antibody target. Whether an autoantibody or antibody against NRARP could matter depends on whether native NRARP is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NRARP 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 NRARP as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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