NOTO
Homeobox protein notochord
Also known as: NOTO_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A8MTQ0
- Gene
- NOTO
- Ensembl
- ENSG00000214513
- Chromosome
- 2
- Canonical length
- 251 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in brain development; neuron differentiation; and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within several processes, including embryonic organ development; motile cilium assembly; and regulation of cilium assembly. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
251 residues, UniProt reviewed canonical sequence.
>A8MTQ0|NOTO
1 MPSPRPRGSP PPAPSGSRVR PPRSGRSPAP RSPTGPNTPR APGRFESPFS VEAILARPDP
61 CAPAASQPSG SACVHPAFWT AASLCATGGL PWACPTSWLP AYLSVGFYPV PGPRVAPVCG
121 LLGFGVTGLE LAHCSGLWAF PDWAPTEDLQ DTERQQKRVR TMFNLEQLEE LEKVFAKQHN
181 LVGKKRAQLA ARLKLTENQV RVWFQNRRVK YQKQQKLRAA VTSAEAASLD EPSSSSIASI
241 QSDDAESGVD GLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NOTO 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)
- 0.64
- Highest tissue expression
- 0.4 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 0.4 nTPM
- skin: 0.2 nTPM
- adrenal gland: 0.1 nTPM
- appendix: 0.1 nTPM
- duodenum: 0.1 nTPM
- parathyroid gland: 0.1 nTPM
Single-cell type
- epididymal basal cells: 1.4 nCPM
- syncytiotrophoblasts: 1.2 nCPM
- gastric chief cells: 1.1 nCPM
- undifferentiated spermatogonia: 1.1 nCPM
- late spermatids: 0.5 nCPM
- early spermatids: 0.4 nCPM
Immune cell
- basophil: 0.4 nTPM
- neutrophil: 0.3 nTPM
- NK-cell: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
- memory CD4 T-cell: 0.1 nTPM
Brain region
- cerebellum: 1.9 nTPM
- medulla oblongata: 1.7 nTPM
- pons: 1.6 nTPM
- midbrain: 1.5 nTPM
- cerebral cortex: 1.4 nTPM
- amygdala: 1.3 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)
- 1.33
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- -0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- brain development
- central nervous system development
- dorsal/ventral pattern formation
- embryonic pattern specification
- heart looping
- motile cilium assembly
- neuron differentiation
- notochord development
- regulation of cilium assembly
- regulation of transcription by RNA polymerase II
Molecular functions
- 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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads NOTO as an antibody target. Whether an autoantibody or antibody against NOTO could matter depends on whether native NOTO is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NOTO 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 NOTO as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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