Seroatlas · Human Serome Atlas

NIT2

Omega-amidase NIT2

Also known as: NIT2_HUMAN

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9NQR4
Gene
NIT2
Ensembl
ENSG00000114021
Chromosome
3
Canonical length
276 aa
Protein class
Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
Subcellular location
Centrosome,Cytosol
Quaternary structure
Homodimer

OverviewNCBI Gene

Enables omega-amidase activity. Involved in asparagine metabolic process; glutamine metabolic process; and oxaloacetate metabolic process. Located in centrosome and cytosol. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

276 residues, UniProt reviewed canonical sequence.

>Q9NQR4|NIT2
     1  MTSFRLALIQ LQISSIKSDN VTRACSFIRE AATQGAKIVS LPECFNSPYG AKYFPEYAEK
    61  IPGESTQKLS EVAKECSIYL IGGSIPEEDA GKLYNTCAVF GPDGTLLAKY RKIHLFDIDV
   121  PGKITFQESK TLSPGDSFST FDTPYCRVGL GICYDMRFAE LAQIYAQRGC QLLVYPGAFN
   181  LTTGPAHWEL LQRSRAVDNQ VYVATASPAR DDKASYVAWG HSTVVNPWGE VLAKAGTEEA
   241  IVYSDIDLKK LAEIRQQIPV FRQKRSDLYA VEMKKP

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against NIT2 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)
0.22
Highest tissue expression
25 nTPM

Expression across tissuesHPA

Tissue

  • liver: 25 nTPM
  • kidney: 17 nTPM
  • skeletal muscle: 8.7 nTPM
  • tongue: 7.1 nTPM
  • breast: 6.4 nTPM
  • thyroid gland: 5.5 nTPM

Single-cell type

  • hepatocytes: 220 nCPM
  • gastric progenitor cells: 147 nCPM
  • esophageal suprabasal cells: 132 nCPM
  • esophageal basal cells: 125 nCPM
  • decidual stromal cells: 117 nCPM
  • cytotrophoblasts: 112 nCPM

Immune cell

  • myeloid DC: 2 nTPM
  • memory B-cell: 1.5 nTPM
  • naive B-cell: 1.5 nTPM
  • MAIT T-cell: 1.4 nTPM
  • naive CD4 T-cell: 1.2 nTPM
  • T-reg: 1.2 nTPM

Brain region

  • basal ganglia: 9.2 nTPM
  • cerebral cortex: 8.1 nTPM
  • choroid plexus: 7.9 nTPM
  • cerebellum: 7 nTPM
  • hypothalamus: 7 nTPM
  • white matter: 6.9 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)
1.77
gnomAD pLI
0
gnomAD missense Z
0.4
DepMap mean gene effect
-0.14
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

  • 2-oxoglutaramate amidase activity
  • omega-amidase activity

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads NIT2 as an antibody target. Whether an autoantibody or antibody against NIT2 could matter depends on whether native NIT2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

NIT2 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 NIT2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/NIT2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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