MBD6
Methyl-CpG-binding domain protein 6
Also known as: KIAA1887, MBD6_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96DN6
- Gene
- MBD6
- Ensembl
- ENSG00000166987
- Chromosome
- 12
- Canonical length
- 1003 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables chromatin binding activity. Located in chromocenter; fibrillar center; and nucleoplasm. Implicated in autism spectrum disorder. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
1003 residues, UniProt reviewed canonical sequence.
>Q96DN6|MBD6
1 MNGGNESSGA DRAGGPVATS VPIGWQRCVR EGAVLYISPS GTELSSLEQT RSYLLSDGTC
61 KCGLECPLNV PKVFNFDPLA PVTPGGAGVG PASEEDMTKL CNHRRKAVAM ATLYRSMETT
121 CSHSSPGEGA SPQMFHTVSP GPPSARPPCR VPPTTPLNGG PGSLPPEPPS VSQAFPTLAG
181 PGGLFPPRLA DPVPSGGSSS PRFLPRGNAP SPAPPPPPAI SLNAPSYNWG AALRSSLVPS
241 DLGSPPAPHA SSSPPSDPPL FHCSDALTPP PLPPSNNLPA HPGPASQPPV SSATMHLPLV
301 LGPLGGAPTV EGPGAPPFLA SSLLSAAAKA QHPPLPPPST LQGRRPRAQA PSASHSSSLR
361 PSQRRPRRPP TVFRLLEGRG PQTPRRSRPR APAPVPQPFS LPEPSQPILP SVLSLLGLPT
421 PGPSHSDGSF NLLGSDAHLP PPPTLSSGSP PQPRHPIQPS LPGTTSGSLS SVPGAPAPPA
481 ASKAPVVPSP VLQSPSEGLG MGAGPACPLP PLAGGEAFPF PSPEQGLALS GAGFPGMLGA
541 LPLPLSLGQP PPSPLLNHSL FGVLTGGGGQ PPPEPLLPPP GGPGPPLAPG EPEGPSLLVA
601 SLLPPPPSDL LPPPSAPPSN LLASFLPLLA LGPTAGDGEG SAEGAGGPSG EPFSGLGDLS
661 PLLFPPLSAP PTLIALNSAL LAATLDPPSG TPPQPCVLSA PQPGPPTSSV TTATTDPGAS
721 SLGKAPSNSG RPPQLLSPLL GASLLGDLSS LTSSPGALPS LLQPPGPLLS GQLGLQLLPG
781 GGAPPPLSEA SSPLACLLQS LQIPPEQPEA PCLPPESPAS ALEPEPARPP LSALAPPHGS
841 PDPPVPELLT GRGSGKRGRR GGGGLRGING EARPARGRKP GSRREPGRLA LKWGTRGGFN
901 GQMERSPRRT HHWQHNGELA EGGAEPKDPP PPGPHSEDLK VPPGVVRKSR RGRRRKYNPT
961 RNSNSSRQDI TLEPSPTARA AVPLPPRARP GRPAKNKRRK LAPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MBD6 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)
- 0.71
- Highest tissue expression
- 103 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 103 nTPM
- pituitary gland: 96 nTPM
- spleen: 59 nTPM
- testis: 54 nTPM
- bone marrow: 54 nTPM
- endometrium: 45 nTPM
Single-cell type
- neutrophils: 194 nCPM
- platelets: 64 nCPM
- early primary spermatocytes: 59 nCPM
- tuft cells: 58 nCPM
- neutrophil progenitors: 54 nCPM
- pituicytes/fscs: 51 nCPM
Immune cell
- neutrophil: 14 nTPM
- gdT-cell: 1.3 nTPM
- memory B-cell: 1.3 nTPM
- classical monocyte: 1 nTPM
- intermediate monocyte: 0.9 nTPM
- naive B-cell: 0.8 nTPM
Brain region
- white matter: 53 nTPM
- thalamus: 50 nTPM
- medulla oblongata: 49 nTPM
- cerebral cortex: 47 nTPM
- hypothalamus: 45 nTPM
- choroid plexus: 44 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)
- 0.21
- gnomAD pLI
- 1
- gnomAD missense Z
- -0.74
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MBD6 as an antibody target. Whether an autoantibody or antibody against MBD6 could matter depends on whether native MBD6 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MBD6 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 MBD6 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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