PRDM14
PR domain zinc finger protein 14
Also known as: PRD14_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9GZV8
- Gene
- PRDM14
- Ensembl
- ENSG00000147596
- Chromosome
- 8
- Canonical length
- 571 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
This gene encodes a member of the PRDI-BF1 and RIZ homology domain containing (PRDM) family of transcriptional regulators. The encoded protein may possess histone methyltransferase activity and plays a critical role in cell pluripotency by suppressing the expression of differentiation marker genes. Expression of this gene may play a role in breast cancer. [provided by RefSeq, Dec 2011]
Canonical amino-acid sequenceUniProt
571 residues, UniProt reviewed canonical sequence.
>Q9GZV8|PRDM14
1 MALPRPSEAV PQDKVCYPPE SSPQNLAAYY TPFPSYGHYR NSLATVEEDF QPFRQLEAAA
61 SAAPAMPPFP FRMAPPLLSP GLGLQREPLY DLPWYSKLPP WYPIPHVPRE VPPFLSSSHE
121 YAGASSEDLG HQIIGGDNES GPCCGPDTLI PPPPADASLL PEGLRTSQLL PCSPSKQSED
181 GPKPSNQEGK SPARFQFTEE DLHFVLYGVT PSLEHPASLH HAISGLLVPP DSSGSDSLPQ
241 TLDKDSLQLP EGLCLMQTVF GEVPHFGVFC SSFIAKGVRF GPFQGKVVNA SEVKTYGDNS
301 VMWEIFEDGH LSHFIDGKGG TGNWMSYVNC ARFPKEQNLV AVQCQGHIFY ESCKEIHQNQ
361 ELLVWYGDCY EKFLDIPVSL QVTEPGKQPS GPSEESAEGY RCERCGKVFT YKYYRDKHLK
421 YTPCVDKGDR KFPCSLCKRS FEKRDRLRIH ILHVHEKHRP HKCSTCGKCF SQSSSLNKHM
481 RVHSGDRPYQ CVYCTKRFTA SSILRTHIRQ HSGEKPFKCK YCGKSFASHA AHDSHVRRSH
541 KEDDGCSCSI CGKIFSDQET FYSHMKFHED YLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRDM14 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)
- 0.49
- Highest tissue expression
- 0.7 nTPM
Expression across tissuesHPA
Tissue
- testis: 0.7 nTPM
- bone marrow: 0.2 nTPM
- choroid plexus: 0.2 nTPM
- retina: 0.2 nTPM
- duodenum: 0.1 nTPM
- epididymis: 0.1 nTPM
Single-cell type
- hepatic stellate cells: 6.5 nCPM
- thymocytes: 3.4 nCPM
- undifferentiated spermatogonia: 2.6 nCPM
- cone photoreceptor cells: 2.1 nCPM
- breast secretory cells: 0.7 nCPM
- endometrial stromal cells: 0.7 nCPM
Immune cell
- neutrophil: 0.1 nTPM
- non-classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebellum: 2.1 nTPM
- white matter: 2 nTPM
- cerebral cortex: 1.8 nTPM
- choroid plexus: 1.8 nTPM
- medulla oblongata: 1.6 nTPM
- pons: 1.6 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)
- 0.6
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.88
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell fate specification
- cell morphogenesis
- embryo implantation
- fertilization
- fibroblast growth factor receptor signaling pathway
- germ cell development
- germ-line stem cell population maintenance
- homeostasis of number of cells within a tissue
- inner cell mass cell fate commitment
- methylation
- negative regulation of fibroblast growth factor receptor signaling pathway
- negative regulation of gene expression, epigenetic
- negative regulation of transcription by RNA polymerase II
- positive regulation of flagellated sperm motility
- positive regulation of stem cell population maintenance
- regulation of transcription by RNA polymerase II
Molecular functions
- chromatin DNA binding
- histone methyltransferase binding
- methyltransferase activity
- RNA binding
- RNA polymerase II transcription regulatory region sequence-specific DNA binding
- zinc ion binding
- methyltransferase regulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PRDM14 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 PRDM14 as an antibody target. Whether an autoantibody or antibody against PRDM14 could matter depends on whether native PRDM14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRDM14 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 PRDM14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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