TDRKH
Tudor and KH domain-containing protein
Also known as: TDRD2, TDRKH_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2W6
- Gene
- TDRKH
- Ensembl
- ENSG00000182134
- Chromosome
- 1
- Canonical length
- 561 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Centrosome,Cytosol
OverviewNCBI Gene
Predicted to enable RNA binding activity. Predicted to be involved in several processes, including P granule organization; male meiotic nuclear division; and piRNA processing. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
561 residues, UniProt reviewed canonical sequence.
>Q9Y2W6|TDRKH
1 MSTERTSWTS LSTIQKIALG LGIPASATVA YILYRRYRES REERLTFVGE DDIEIEMRVP
61 QEAVKLIIGR QGANIKQLRK QTGARIDVDT EDVGDERVLL ISGFPVQVCK AKAAIHQILT
121 ENTPVSEQLS VPQRSVGRII GRGGETIRSI CKASGAKITC DKESEGTLLL SRLIKISGTQ
181 KEVAAAKHLI LEKVSEDEEL RKRIAHSAET RVPRKQPISV RREDMTEPGG AGEPALWKNT
241 SSSMEPTAPL VTPPPKGGGD MAVVVSKEGS WEKPSDDSFQ KSEAQAIPEM PMFEIPSPDF
301 SFHADEYLEV YVSASEHPNH FWIQIVGSRS LQLDKLVNEM TQHYENSVPE DLTVHVGDIV
361 AAPLPTNGSW YRARVLGTLE NGNLDLYFVD FGDNGDCPLK DLRALRSDFL SLPFQAIECS
421 LARIAPSGDQ WEEEALDEFD RLTHCADWKP LVAKISSYVQ TGISTWPKIY LYDTSNGKKL
481 DIGLELVHKG YAIELPEDIE ENRAVPDMLK DMATETDASL STLLTETKKS SGEITHTLSC
541 LSLSEAASMS GDDNLEDDYL LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TDRKH 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)
- 0.42
- Highest tissue expression
- 28 nTPM
Expression across tissuesHPA
Tissue
- parathyroid gland: 28 nTPM
- testis: 21 nTPM
- cerebellum: 13 nTPM
- thymus: 9.4 nTPM
- retina: 8.9 nTPM
- cerebral cortex: 7.2 nTPM
Single-cell type
- late spermatids: 112 nCPM
- oocytes: 83 nCPM
- early primary spermatocytes: 61 nCPM
- breast lactating cells: 47 nCPM
- platelets: 47 nCPM
- late primary spermatocytes: 47 nCPM
Immune cell
- MAIT T-cell: 13 nTPM
- T-reg: 10 nTPM
- memory CD8 T-cell: 8.3 nTPM
- gdT-cell: 8.2 nTPM
- non-classical monocyte: 8.1 nTPM
- NK-cell: 7.7 nTPM
Brain region
- pons: 18 nTPM
- cerebellum: 17 nTPM
- medulla oblongata: 14 nTPM
- hypothalamus: 13 nTPM
- thalamus: 12 nTPM
- midbrain: 12 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TDRKH.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 68 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.52
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 1.8
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 15% 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
- Tudor domain
- K Homology domain
- K Homology domain, type 1
- SNase-like, OB-fold superfamily
- K Homology domain, type 1 superfamily
- Tudor domain-containing
- KH domain
- Tudor domain
- Tudor domain-containing protein 2-like, tudor domain
- Tudor and KH domain-containing protein, second type I K homology domain
- Tudor and KH domain-containing protein, first type I K homology domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TDRKH as an antibody target. Whether an autoantibody or antibody against TDRKH could matter depends on whether native TDRKH is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TDRKH 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 TDRKH as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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