KLHL23
Kelch-like protein 23
Also known as: FLJ37812, KLH23_HUMAN, MGC22679, MGC2610
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NBE8
- Gene
- KLHL23
- Ensembl
- ENSG00000213160
- Chromosome
- 2
- Canonical length
- 558 aa
- Protein class
- Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Actin filaments
OverviewNCBI Gene
This locus represents naturally occurring read-through transcription between the neighboring PHOSPHO2 (phosphatase, orphan 2) and KLHL23 (kelch-like 23) genes on chromosome 2. The read-through transcript includes only non-coding PHOSPHO2 exons, and thus encodes the KLHL23 protein. [provided by RefSeq, Dec 2010]
Canonical amino-acid sequenceUniProt
558 residues, UniProt reviewed canonical sequence.
>Q8NBE8|KLHL23
1 MALKGQEDYI YLFKDSTHPV DFLDAFRTFY LDGLFTDITL QCPSGIIFHC HRAVLAACSN
61 YFKAMFTADM KEKFKNKIKL SGIHHDILEG LVNYAYTSQI EITKRNVQSL LEAADLLQFL
121 SVKKACERFL VRHLDIDNCI GMHSFAEFHV CPELEKESRR ILCSKFKEVW QQEEFLEISL
181 EKFLFILSRK NLSVWKEEAI IEPVIKWTAH DVENRIECLY NLLSYINIDI DPVYLKTALG
241 LQRSCLLTEN KIRSLIYNAL NPMHKEISQR STATMYIIGG YYWHPLSEVH IWDPLTNVWI
301 QGAEIPDYTR ESYGVTCLGP NIYVTGGYRT DNIEALDTVW IYNSESDEWT EGLPMLNARY
361 YHCAVTLGGC VYALGGYRKG APAEEAEFYD PLKEKWIPIA NMIKGVGNAT ACVLHDVIYV
421 IGGHCGYRGS CTYDKVQSYN SDINEWSLIT SSPHPEYGLC SVPFENKLYL VGGQTTITEC
481 YDPEQNEWRE IAPMMERRME CGAVIMNGCI YVTGGYSYSK GTYLQSIEKY DPDLNKWEIV
541 GNLPSAMRSH GCVCVYNVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KLHL23 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)
- 0.25
- Highest tissue expression
- 24 nTPM
Expression across tissuesHPA
Tissue
- endometrium: 24 nTPM
- smooth muscle: 23 nTPM
- colon: 19 nTPM
- ovary: 19 nTPM
- tongue: 15 nTPM
- cerebral cortex: 14 nTPM
Single-cell type
- retinal bipolar cells: 244 nCPM
- cone photoreceptor cells: 201 nCPM
- vascular smooth muscle cells: 187 nCPM
- pericytes: 166 nCPM
- oligodendrocyte progenitor cells: 161 nCPM
- bergmann glia: 145 nCPM
Immune cell
- NK-cell: 3.4 nTPM
- naive CD4 T-cell: 1 nTPM
- naive CD8 T-cell: 1 nTPM
- MAIT T-cell: 0.9 nTPM
- plasmacytoid DC: 0.9 nTPM
- T-reg: 0.8 nTPM
Brain region
- cerebellum: 37 nTPM
- cerebral cortex: 30 nTPM
- hippocampal formation: 30 nTPM
- basal ganglia: 29 nTPM
- hypothalamus: 25 nTPM
- amygdala: 25 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)
- 0.65
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.73
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- BTB/POZ domain
- Kelch repeat type 1
- SKP1/BTB/POZ domain superfamily
- BTB/Kelch-associated
- Kelch-type beta-propeller
- BTB-kelch protein
- BTB/POZ domain
- Kelch motif
- BTB And C-terminal Kelch
- KLHDC2/KLHL20/DRC7 Kelch-repeats domain
- Kelch-like protein 23, BTB/POZ domain
- Kelch-like protein 23, BACK domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KLHL23 as an antibody target. Whether an autoantibody or antibody against KLHL23 could matter depends on whether native KLHL23 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KLHL23 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 KLHL23 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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