KLHL8
Kelch-like protein 8
Also known as: KIAA1378, KLHL8_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P2G9
- Gene
- KLHL8
- Ensembl
- ENSG00000145332
- Chromosome
- 4
- Canonical length
- 620 aa
- Protein class
- Cancer-related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable ubiquitin-like ligase-substrate adaptor activity. Involved in protein ubiquitination and ubiquitin-dependent protein catabolic process. Located in nucleoplasm. Part of Cul3-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
620 residues, UniProt reviewed canonical sequence.
>Q9P2G9|KLHL8
1 MASDSMSSKQ ARNHITKGKR QQQHQQIKNR SSISDGDGED SFIFEANEAW KDFHGSLLRF
61 YENGELCDVT LKVGSKLISC HKLVLACVIP YFRAMFLSEM AEAKQTLIEI RDFDGDAIED
121 LVKFVYSSRL TLTVDNVQPL LYAACILQVE LVARACCEYM KLHFHPSNCL AVRAFAESHN
181 RIDLMDMADQ YACDHFTEVV ECEDFVSVSP QHLHKLLSSS DLNIENEKQV YNAAIKWLLA
241 NPQHHSKWLD ETLAQVRLPL LPVDFLMGVV AKEQIVKQNL KCRDLLDEAR NYHLHLSSRA
301 VPDFEYSIRT TPRKHTAGVL FCVGGRGGSG DPFRSIECYS INKNSWFFGP EMNSRRRHVG
361 VISVEGKVYA VGGHDGNEHL GSMEMFDPLT NKWMMKASMN TKRRGIALAS LGGPIYAIGG
421 LDDNTCFNDV ERYDIESDQW STVAPMNTPR GGVGSVALVN HVYAVGGNDG MASLSSVERY
481 DPHLDKWIEV KEMGQRRAGN GVSKLHGCLY VVGGFDDNSP LSSVERYDPR SNKWDYVAAL
541 TTPRGGVGIA TVMGKIFAVG GHNGNAYLNT VEAFDPVLNR WELVGSVSHC RAGAGVAVCS
601 CLTSQIRDVG HGSNNVVDCMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KLHL8 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)
- 0.28
- Highest tissue expression
- 57 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 57 nTPM
- retina: 25 nTPM
- thyroid gland: 18 nTPM
- skeletal muscle: 13 nTPM
- kidney: 11 nTPM
- liver: 11 nTPM
Single-cell type
- müller glia: 596 nCPM
- epididymal principal cells: 323 nCPM
- renal collecting duct principal cells: 310 nCPM
- neutrophils: 282 nCPM
- monocyte progenitors: 147 nCPM
- rod photoreceptor cells: 128 nCPM
Immune cell
- classical monocyte: 12 nTPM
- myeloid DC: 10 nTPM
- non-classical monocyte: 9.8 nTPM
- intermediate monocyte: 9.2 nTPM
- neutrophil: 8.6 nTPM
- NK-cell: 8.4 nTPM
Brain region
- cerebellum: 19 nTPM
- hypothalamus: 17 nTPM
- midbrain: 16 nTPM
- white matter: 15 nTPM
- thalamus: 15 nTPM
- spinal cord: 14 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)
- 0.75
- gnomAD pLI
- 0
- gnomAD missense Z
- 2.23
- DepMap mean gene effect
- 0.11
- 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
- proteasome-mediated ubiquitin-dependent protein catabolic process
- protein ubiquitination
- ubiquitin-dependent protein catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KLHL8 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 KLHL8 as an antibody target. Whether an autoantibody or antibody against KLHL8 could matter depends on whether native KLHL8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KLHL8 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 KLHL8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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