HYPK
Huntingtin-interacting protein K
Also known as: C15orf63, FLJ20431, HSPC136, HYPK_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NX55
- Gene
- HYPK
- Ensembl
- ENSG00000242028
- Chromosome
- 15
- Canonical length
- 121 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Microtubules
OverviewNCBI Gene
Enables protein folding chaperone. Involved in negative regulation of apoptotic process and protein stabilization. Located in cytoplasm; microtubule cytoskeleton; and nucleoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
121 residues, UniProt reviewed canonical sequence.
>Q9NX55|HYPK
1 MATEGDVELE LETETSGPER PPEKPRKHDS GAADLERVTD YAEEKEIQSS NLETAMSVIG
61 DRRSREQKAK QEREKELAKV TIKKEDLELI MTEMEISRAA AERSLREHMG NVVEALIALT
121 NLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HYPK 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)
- 0.53
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- choroid plexus: 25 nTPM
- skeletal muscle: 23 nTPM
- heart muscle: 16 nTPM
- tongue: 14 nTPM
- spinal cord: 14 nTPM
- midbrain: 13 nTPM
Single-cell type
- oligodendrocytes: 28 nCPM
- other brain neurons: 26 nCPM
- brain excitatory neurons: 25 nCPM
- brain inhibitory neurons: 24 nCPM
- astrocytes: 20 nCPM
- oligodendrocyte progenitor cells: 19 nCPM
Immune cell
- non-classical monocyte: 48 nTPM
- plasmacytoid DC: 40 nTPM
- intermediate monocyte: 38 nTPM
- naive B-cell: 32 nTPM
- memory B-cell: 30 nTPM
- naive CD4 T-cell: 30 nTPM
Brain region
- cerebellum: 18 nTPM
- midbrain: 16 nTPM
- white matter: 16 nTPM
- cerebral cortex: 15 nTPM
- hypothalamus: 15 nTPM
- pons: 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)
- 1.21
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 0.74
- DepMap mean gene effect
- -0.87
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Nascent polypeptide-associated complex subunit alpha-like, UBA domain
- HYPK UBA domain
- Huntingtin-interacting protein K, UBA-like domain
- Huntingtin-interacting protein K
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of HYPK 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 HYPK as an antibody target. Whether an autoantibody or antibody against HYPK could matter depends on whether native HYPK is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HYPK 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 HYPK as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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