MIS12
Protein MIS12 homolog
Also known as: hMIS12, KNTC2AP, MGC2488, MIS12_HUMAN, MTW1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H081
- Gene
- MIS12
- Ensembl
- ENSG00000167842
- Chromosome
- 17
- Canonical length
- 205 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Involved in attachment of mitotic spindle microtubules to kinetochore and kinetochore assembly. Located in kinetochore and nucleus. Part of MIS12/MIND type complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
205 residues, UniProt reviewed canonical sequence.
>Q9H081|MIS12
1 MSVDPMTYEA QFFGFTPQTC MLRIYIAFQD YLFEVMQAVE QVILKKLDGI PDCDISPVQI
61 RKCTEKFLCF MKGHFDNLFS KMEQLFLQLI LRIPSNILLP EDKCKETPYS EEDFQHLQKE
121 IEQLQEKYKT ELCTKQALLA ELEEQKIVQA KLKQTLTFFD ELHNVGRDHG TSDFRESLVS
181 LVQNSRKLQN IRDNVEKESK RLKISLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MIS12 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
- 30 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 30 nTPM
- retina: 26 nTPM
- thymus: 24 nTPM
- lymph node: 20 nTPM
- tonsil: 20 nTPM
- thyroid gland: 18 nTPM
Single-cell type
- late spermatids: 425 nCPM
- epididymal principal cells: 254 nCPM
- early spermatids: 120 nCPM
- late primary spermatocytes: 95 nCPM
- epididymal basal cells: 58 nCPM
- cone photoreceptor cells: 50 nCPM
Immune cell
- NK-cell: 16 nTPM
- MAIT T-cell: 16 nTPM
- naive CD4 T-cell: 16 nTPM
- naive CD8 T-cell: 15 nTPM
- gdT-cell: 15 nTPM
- memory CD8 T-cell: 14 nTPM
Brain region
- white matter: 24 nTPM
- medulla oblongata: 18 nTPM
- basal ganglia: 18 nTPM
- midbrain: 16 nTPM
- pons: 16 nTPM
- cerebral cortex: 16 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)
- 1.07
- gnomAD pLI
- 0.15
- gnomAD missense Z
- 0.64
- DepMap mean gene effect
- -1.12
- DepMap dependency class
- common
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
- attachment of mitotic spindle microtubules to kinetochore
- attachment of spindle microtubules to kinetochore
- cell division
- chromosome segregation
- kinetochore assembly
- mitotic sister chromatid segregation
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Centromere protein Mis12
- Mis12 protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MIS12 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 MIS12 as an antibody target. Whether an autoantibody or antibody against MIS12 could matter depends on whether native MIS12 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MIS12 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 MIS12 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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