KDM5D
Lysine-specific demethylase 5D
Also known as: HY, HYA, JARID1D, KDM5D_HUMAN, KIAA0234, SMCY
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BY66
- Gene
- KDM5D
- Ensembl
- ENSG00000012817
- Chromosome
- Y
- Canonical length
- 1539 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoli fibrillar center
OverviewNCBI Gene
This gene encodes a protein containing zinc finger domains. A short peptide derived from this protein is a minor histocompatibility antigen which can lead to graft rejection of male donor cells in a female recipient. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]
Canonical amino-acid sequenceUniProt
1539 residues, UniProt reviewed canonical sequence.
>Q9BY66|KDM5D
1 MEPGCDEFLP PPECPVFEPS WAEFQDPLGY IAKIRPIAEK SGICKIRPPA DWQPPFAVEV
61 DNFRFTPRVQ RLNELEAQTR VKLNYLDQIA KFWEIQGSSL KIPNVERKIL DLYSLSKIVI
121 EEGGYEAICK DRRWARVAQR LHYPPGKNIG SLLRSHYERI IYPYEMFQSG ANHVQCNTHP
181 FDNEVKDKEY KPHSIPLRQS VQPSKFSSYS RRAKRLQPDP EPTEEDIEKH PELKKLQIYG
241 PGPKMMGLGL MAKDKDKTVH KKVTCPPTVT VKDEQSGGGN VSSTLLKQHL SLEPCTKTTM
301 QLRKNHSSAQ FIDSYICQVC SRGDEDDKLL FCDGCDDNYH IFCLLPPLPE IPRGIWRCPK
361 CILAECKQPP EAFGFEQATQ EYSLQSFGEM ADSFKSDYFN MPVHMVPTEL VEKEFWRLVS
421 SIEEDVTVEY GADIHSKEFG SGFPVSNSKQ NLSPEEKEYA TSGWNLNVMP VLDQSVLCHI
481 NADISGMKVP WLYVGMVFSA FCWHIEDHWS YSINYLHWGE PKTWYGVPSL AAEHLEEVMK
541 MLTPELFDSQ PDLLHQLVTL MNPNTLMSHG VPVVRTNQCA GEFVITFPRA YHSGFNQGYN
601 FAEAVNFCTA DWLPAGRQCI EHYRRLRRYC VFSHEELICK MAAFPETLDL NLAVAVHKEM
661 FIMVQEERRL RKALLEKGVT EAEREAFELL PDDERQCIKC KTTCFLSALA CYDCPDGLVC
721 LSHINDLCKC SSSRQYLRYR YTLDELPTML HKLKIRAESF DTWANKVRVA LEVEDGRKRS
781 FEELRALESE ARERRFPNSE LLQRLKNCLS EVEACIAQVL GLVSGQVARM DTPQLTLTEL
841 RVLLEQMGSL PCAMHQIGDV KDVLEQVEAY QAEAREALAT LPSSPGLLRS LLERGQQLGV
901 EVPEAHQLQQ QVEQAQWLDE VKQALAPSAH RGSLVIMQGL LVMGAKIASS PSVDKARAEL
961 QELLTIAERW EEKAHFCLEA RQKHPPATLE AIIRETENIP VHLPNIQALK EALTKAQAWI
1021 ADVDEIQNGD HYPCLDDLEG LVAVGRDLPV GLEELRQLEL QVLTAHSWRE KASKTFLKKN
1081 SCYTLLEVLC PCADAGSDST KRSRWMEKAL GLYQCDTELL GLSAQDLRDP GSVIVAFKEG
1141 EQKEKEGILQ LRRTNSAKPS PLAPSLMASS PTSICVCGQV PAGVGVLQCD LCQDWFHGQC
1201 VSVPHLLTSP KPSLTSSPLL AWWEWDTKFL CPLCMRSRRP RLETILALLV ALQRLPVRLP
1261 EGEALQCLTE RAIGWQDRAR KALASEDVTA LLRQLAELRQ QLQAKPRPEE ASVYTSATAC
1321 DPIREGSGNN ISKVQGLLEN GDSVTSPENM APGKGSDLEL LSSLLPQLTG PVLELPEAIR
1381 APLEELMMEG DLLEVTLDEN HSIWQLLQAG QPPDLDRIRT LLELEKFEHQ GSRTRSRALE
1441 RRRRRQKVDQ GRNVENLVQQ ELQSKRARSS GIMSQVGREE EHYQEKADRE NMFLTPSTDH
1501 SPFLKGNQNS LQHKDSGSSA ACPSLMPLLQ LSYSDEQQLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KDM5D 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)
- 0.34
- Highest tissue expression
- 33 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 33 nTPM
- adrenal gland: 30 nTPM
- spleen: 29 nTPM
- prostate: 25 nTPM
- tongue: 24 nTPM
- colon: 22 nTPM
Single-cell type
- retinal bipolar cells: 92 nCPM
- leydig cells: 85 nCPM
- myonuclei: 84 nCPM
- oligodendrocytes: 80 nCPM
- choroid plexus epithelial cells: 78 nCPM
- retinal amacrine cells: 72 nCPM
Immune cell
- memory B-cell: 3.2 nTPM
- naive B-cell: 2.6 nTPM
- plasmacytoid DC: 2.6 nTPM
- naive CD4 T-cell: 2.4 nTPM
- gdT-cell: 2.3 nTPM
- memory CD4 T-cell: 2.2 nTPM
Brain region
- choroid plexus: 15 nTPM
- white matter: 13 nTPM
- medulla oblongata: 12 nTPM
- cerebral cortex: 12 nTPM
- cerebellum: 11 nTPM
- pons: 11 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about KDM5D.
Disease | ImmuneIEDB
Conditions an epitope on KDM5D was assayed in.
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)
- 0.36
- gnomAD pLI
- 0.93
- gnomAD missense Z
- -0.37
- DepMap mean gene effect
- 0.4
- DepMap dependency class
- none
OntologyGO
Biological processes
- chromatin remodeling
- regulation of androgen receptor signaling pathway
- regulation of DNA-templated transcription
- T cell antigen processing and presentation
Molecular functions
- DNA binding
- histone demethylase activity
- histone H3K4 demethylase activity
- histone H3K4me/H3K4me2/H3K4me3 demethylase activity
- nuclear androgen receptor binding
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- ARID DNA-binding domain
- Zinc finger, PHD-type
- JmjC domain
- JmjN domain
- Zinc finger, C5HC2-type
- Zinc finger, FYVE/PHD-type
- Zinc finger, RING/FYVE/PHD-type
- Lysine-specific demethylase-like domain
- Zinc finger, PHD-type, conserved site
- Zinc finger, PHD-finger
- ARID DNA-binding domain superfamily
- Lysine-specific demethylase 5, C-terminal helical domain
- PHD-finger
- ARID/BRIGHT DNA binding domain
- JmjC domain, hydroxylase
- jmjN domain
- C5HC2 zinc finger
- PLU-1-like protein
- Lysine-specific demethylase 5, C-terminal helical domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KDM5D 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 KDM5D as an antibody target. Whether an autoantibody or antibody against KDM5D could matter depends on whether native KDM5D is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KDM5D 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 KDM5D as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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