NUDC
Nuclear migration protein nudC
Also known as: NUDC_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y266
- Gene
- NUDC
- Ensembl
- ENSG00000090273
- Chromosome
- 1
- Canonical length
- 331 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene encodes a nuclear distribution protein that plays an essential role in mitosis and cytokinesis. The encoded protein is involved in spindle formation during mitosis and in microtubule organization during cytokinesis. Pseudogenes of this gene are found on chromosome 2. [provided by RefSeq, Feb 2012]
Canonical amino-acid sequenceUniProt
331 residues, UniProt reviewed canonical sequence.
>Q9Y266|NUDC
1 MGGEQEEERF DGMLLAMAQQ HEGGVQELVN TFFSFLRRKT DFFIGGEEGM AEKLITQTFS
61 HHNQLAQKTR REKRARQEAE RREKAERAAR LAKEAKSETS GPQIKELTDE EAERLQLEID
121 QKKDAENHEA QLKNGSLDSP GKQDTEEDEE EDEKDKGKLK PNLGNGADLP NYRWTQTLSE
181 LDLAVPFCVN FRLKGKDMVV DIQRRHLRVG LKGQPAIIDG ELYNEVKVEE SSWLIEDGKV
241 VTVHLEKINK MEWWSRLVSS DPEINTKKIN PENSKLSDLD SETRSMVEKM MYDQRQKSMG
301 LPTSDEQKKQ EILKKFMDQH PEMDFSKAKF NLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NUDC 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)
- 0.44
- Highest tissue expression
- 158 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 158 nTPM
- adrenal gland: 134 nTPM
- cerebral cortex: 126 nTPM
- skeletal muscle: 122 nTPM
- amygdala: 113 nTPM
- liver: 112 nTPM
Single-cell type
- hepatocytes: 735 nCPM
- fallopian tube ciliated cells: 734 nCPM
- respiratory ciliated cells: 621 nCPM
- epididymal efferent duct ciliated cells: 518 nCPM
- endometrial ciliated cells: 487 nCPM
- differentiating spermatogonia: 329 nCPM
Immune cell
- naive B-cell: 187 nTPM
- basophil: 185 nTPM
- memory B-cell: 177 nTPM
- total PBMC: 168 nTPM
- T-reg: 164 nTPM
- plasmacytoid DC: 164 nTPM
Brain region
- cerebral cortex: 93 nTPM
- choroid plexus: 88 nTPM
- white matter: 88 nTPM
- hypothalamus: 81 nTPM
- cerebellum: 76 nTPM
- pons: 72 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)
- 0.38
- gnomAD pLI
- 0.89
- gnomAD missense Z
- 0.79
- DepMap mean gene effect
- -0.75
- DepMap dependency class
- common
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
- cell division
- mitotic metaphase chromosome alignment
- mitotic spindle organization
- nuclear migration
- protein folding
- response to peptide hormone
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- CS domain
- HSP20-like chaperone
- NudC N-terminal domain
- NudC family
- CS domain
- N-terminal conserved domain of Nudc.
- Nuclear migration protein nudC
- Nuclear distribution C domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NUDC 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 NUDC as an antibody target. Whether an autoantibody or antibody against NUDC could matter depends on whether native NUDC is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NUDC 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 NUDC as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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