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Aliases for PHF8 Gene

Aliases for PHF8 Gene

  • PHD Finger Protein 8 2 3 4 5
  • Jumonji C Domain-Containing Histone Demethylase 1F 2 3
  • EC 1.14.11.27 4 58
  • ZNF422 3 4
  • Histone Lysine Demethylase PHF8 3
  • KIAA1111 4
  • JHDM1F 3
  • MRXSSD 3
  • KDM7B 3

External Ids for PHF8 Gene

Previous GeneCards Identifiers for PHF8 Gene

  • GC0XM052930
  • GC0XM053846
  • GC0XM051017

Summaries for PHF8 Gene

Entrez Gene Summary for PHF8 Gene

  • The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. The protein has an N-terminal PHD finger and a central Jumonji C domain. This gene is thought to function as a transcription activator. Defects in this gene are a cause of syndromic X-linked Siderius type intellectual disability (MRXSSD) and over-expression of this gene is associated with several forms of cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]

GeneCards Summary for PHF8 Gene

PHF8 (PHD Finger Protein 8) is a Protein Coding gene. Diseases associated with PHF8 include X-Linked Intellectual Disability, Siderius Type and Alacrima, Achalasia, And Mental Retardation Syndrome. Among its related pathways are Cell Cycle, Mitotic and Chromatin organization. GO annotations related to this gene include chromatin binding and methylated histone binding. An important paralog of this gene is PHF2.

UniProtKB/Swiss-Prot for PHF8 Gene

  • Histone lysine demethylase with selectivity for the di- and monomethyl states that plays a key role cell cycle progression, rDNA transcription and brain development. Demethylates mono- and dimethylated histone H3 Lys-9 residue (H3K9Me1 and H3K9Me2), dimethylated H3 Lys-27 (H3K27Me2) and monomethylated histone H4 Lys-20 residue (H4K20Me1). Acts as a transcription activator as H3K9Me1, H3K9Me2, H3K27Me2 and H4K20Me1 are epigenetic repressive marks. Involved in cell cycle progression by being required to control G1-S transition. Acts as a coactivator of rDNA transcription, by activating polymerase I (pol I) mediated transcription of rRNA genes. Required for brain development, probably by regulating expression of neuron-specific genes. Only has activity toward H4K20Me1 when nucleosome is used as a substrate and when not histone octamer is used as substrate. May also have weak activity toward dimethylated H3 Lys-36 (H3K36Me2), however, the relevance of this result remains unsure in vivo. Specifically binds trimethylated Lys-4 of histone H3 (H3K4me3), affecting histone demethylase specificity: has weak activity toward H3K9Me2 in absence of H3K4me3, while it has high activity toward H3K9me2 when binding H3K4me3.

Gene Wiki entry for PHF8 Gene

Additional gene information for PHF8 Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for PHF8 Gene

Genomics for PHF8 Gene

Regulatory Elements for PHF8 Gene

Enhancers for PHF8 Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH0XH054042 1.1 ENCODE 38.9 +4.6 4567 3.8 PKNOX1 FOXA2 ARNT SIN3A FEZF1 DMAP1 ZNF2 YY1 ZNF766 ZNF143 KDM5C PHF8 ACTG1P10 SMC1A ENSG00000233250 TSPYL2 APEX2 GPR173 KANTR MAGED2
GH0XH054638 1.7 FANTOM5 Ensembl ENCODE 15.9 -591.6 -591620 3.9 PKNOX1 SIN3A DMAP1 ZNF2 YY1 ZNF143 SP3 SP5 REST SREBF1 PHF8 GNL3L APEX2 PGAM4P1 PIR60016
GH0XH053681 1.1 ENCODE 23 +364.6 364587 5.9 HDGF PKNOX1 MLX ARNT ARID4B SIN3A DMAP1 ZNF2 YY1 ZNF207 FAM156B PHF8 KANTR HUWE1 ACTG1P10 ENSG00000233250 TSPYL2 KDM5C FGD1 HSD17B10
GH0XH053071 1.3 Ensembl ENCODE 14.2 +976.5 976523 2.4 HDGF ARID4B SIN3A FEZF1 ZNF2 ZNF121 GLIS2 ZNF143 KLF7 ZNF202 TSPYL2 FAM156B ACTG1P10 PHF8 ENSG00000233250 KANTR KDM5C HUWE1 SMC1A ENSG00000270497
GH0XH054439 1 ENCODE 14.9 -391.5 -391505 1.5 PKNOX1 ATF1 ZFP64 ARID4B SIN3A DMAP1 ZNF2 YY1 ETS1 ZNF143 GNL3L PHF8 HUWE1 TSR2 PIR39642
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around PHF8 on UCSC Golden Path with GeneCards custom track

Genomic Locations for PHF8 Gene

Genomic Locations for PHF8 Gene
chrX:53,936,676-54,048,958
(GRCh38/hg38)
Size:
112,283 bases
Orientation:
Minus strand
chrX:53,963,109-54,075,391
(GRCh37/hg19)

Genomic View for PHF8 Gene

Genes around PHF8 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
PHF8 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for PHF8 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for PHF8 Gene

Proteins for PHF8 Gene

  • Protein details for PHF8 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Q9UPP1-PHF8_HUMAN
    Recommended name:
    Histone lysine demethylase PHF8
    Protein Accession:
    Q9UPP1
    Secondary Accessions:
    • B3KMV4
    • B7Z911
    • Q5H9U5
    • Q5JPR9
    • Q5JPS0
    • Q5JPS2
    • Q5JPS3
    • Q5VUJ4
    • Q7Z6D4
    • Q9HAH2

    Protein attributes for PHF8 Gene

    Size:
    1060 amino acids
    Molecular mass:
    117864 Da
    Cofactor:
    Name=Fe(2+); Xref=ChEBI:CHEBI:29033;
    Quaternary structure:
    • Interacts with POLR1B, UBTF, SETD1A, HCFC1, E2F1 and ZNF711.
    SequenceCaution:
    • Sequence=BAA83063.1; Type=Erroneous initiation; Note=Translation N-terminally shortened.; Evidence={ECO:0000305}; Sequence=BAB13877.1; Type=Erroneous initiation; Note=Translation N-terminally extended.; Evidence={ECO:0000305}; Sequence=CAI45929.1; Type=Erroneous termination; Positions=419; Note=Translated as Arg.; Evidence={ECO:0000305};

    Three dimensional structures from OCA and Proteopedia for PHF8 Gene

    Alternative splice isoforms for PHF8 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for PHF8 Gene

Selected DME Specific Peptides for PHF8 Gene

Q9UPP1:
  • GTSVWYH
  • TDFHIDF

Post-translational modifications for PHF8 Gene

  • Phosphorylation at Ser-69 and Ser-120 are required for dissociation from chromatin and accumulation of H4K20Me1 levels during prophase.
  • Ubiquitination at Lys467, Lys486, and Lys732
  • Modification sites at PhosphoSitePlus

Domains & Families for PHF8 Gene

Gene Families for PHF8 Gene

HGNC:
Human Protein Atlas (HPA):
  • Disease related genes
  • Enzymes
  • Potential drug targets
  • Predicted intracellular proteins

Graphical View of Domain Structure for InterPro Entry

Q9UPP1

UniProtKB/Swiss-Prot:

PHF8_HUMAN :
  • The PHD-type zinc finger mediates the binding to H3K4me3. Binding to H3K4me3 promotes its access to H3K9me2.
  • Belongs to the JHDM1 histone demethylase family. JHDM1D subfamily.
Domain:
  • The PHD-type zinc finger mediates the binding to H3K4me3. Binding to H3K4me3 promotes its access to H3K9me2.
  • The linker region is a critical determinant of demethylase specificity. It enables the active site of JmjC to reach the target H3K9me2 when the PHD-type zinc finger binds to H3K4me3.
Family:
  • Belongs to the JHDM1 histone demethylase family. JHDM1D subfamily.
genes like me logo Genes that share domains with PHF8: view

Function for PHF8 Gene

Molecular function for PHF8 Gene

UniProtKB/Swiss-Prot BiophysicochemicalProperties:
Kinetic parameters: KM=134 uM for histone H3 H3K9Me2 {ECO:0000269 PubMed:20023638}; KM=8 uM for histone H3 H3K4me3 and H3K9Me2 {ECO:0000269 PubMed:20023638};
UniProtKB/Swiss-Prot CatalyticActivity:
Protein N(6),N(6)-dimethyl-L-lysine + 2 2-oxoglutarate + 2 O(2) = protein L-lysine + 2 succinate + 2 formaldehyde + 2 CO(2).
UniProtKB/Swiss-Prot Function:
Histone lysine demethylase with selectivity for the di- and monomethyl states that plays a key role cell cycle progression, rDNA transcription and brain development. Demethylates mono- and dimethylated histone H3 Lys-9 residue (H3K9Me1 and H3K9Me2), dimethylated H3 Lys-27 (H3K27Me2) and monomethylated histone H4 Lys-20 residue (H4K20Me1). Acts as a transcription activator as H3K9Me1, H3K9Me2, H3K27Me2 and H4K20Me1 are epigenetic repressive marks. Involved in cell cycle progression by being required to control G1-S transition. Acts as a coactivator of rDNA transcription, by activating polymerase I (pol I) mediated transcription of rRNA genes. Required for brain development, probably by regulating expression of neuron-specific genes. Only has activity toward H4K20Me1 when nucleosome is used as a substrate and when not histone octamer is used as substrate. May also have weak activity toward dimethylated H3 Lys-36 (H3K36Me2), however, the relevance of this result remains unsure in vivo. Specifically binds trimethylated Lys-4 of histone H3 (H3K4me3), affecting histone demethylase specificity: has weak activity toward H3K9Me2 in absence of H3K4me3, while it has high activity toward H3K9me2 when binding H3K4me3.

Enzyme Numbers (IUBMB) for PHF8 Gene

Phenotypes From GWAS Catalog for PHF8 Gene

Gene Ontology (GO) - Molecular Function for PHF8 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0003682 chromatin binding IDA 20622854
GO:0005506 iron ion binding IDA 20023638
GO:0005515 protein binding IPI 20208542
GO:0008270 zinc ion binding IDA 20023638
GO:0016491 oxidoreductase activity IEA --
genes like me logo Genes that share ontologies with PHF8: view
genes like me logo Genes that share phenotypes with PHF8: view

Human Phenotype Ontology for PHF8 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

miRNA for PHF8 Gene

miRTarBase miRNAs that target PHF8

Clone Products

No data available for Animal Models , Transcription Factor Targets and HOMER Transcription for PHF8 Gene

Localization for PHF8 Gene

Subcellular locations from UniProtKB/Swiss-Prot for PHF8 Gene

Nucleus. Nucleus, nucleolus. Note=Recruited to H3K4me3 sites on chromatin during interphase. Dissociates from chromatin when cells enter mitosis.

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for PHF8 gene
Compartment Confidence
nucleus 5
cytosol 2
cytoskeleton 1

Subcellular locations from the

Human Protein Atlas (HPA)

Gene Ontology (GO) - Cellular Components for PHF8 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005634 nucleus IEA,IDA 19843542
GO:0005654 nucleoplasm TAS --
GO:0005730 nucleolus IEA,IDA 20208542
GO:0031965 nuclear membrane IDA --
genes like me logo Genes that share ontologies with PHF8: view

Pathways & Interactions for PHF8 Gene

genes like me logo Genes that share pathways with PHF8: view

Pathways by source for PHF8 Gene

1 GeneTex pathway for PHF8 Gene
1 BioSystems pathway for PHF8 Gene

Gene Ontology (GO) - Biological Process for PHF8 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000082 G1/S transition of mitotic cell cycle IMP 20622854
GO:0006351 transcription, DNA-templated IEA --
GO:0006355 regulation of transcription, DNA-templated IEA --
GO:0007049 cell cycle IEA --
GO:0007420 brain development ISS --
genes like me logo Genes that share ontologies with PHF8: view

No data available for SIGNOR curated interactions for PHF8 Gene

Drugs & Compounds for PHF8 Gene

(5) Drugs for PHF8 Gene - From: ApexBio, DGIdb, and HMDB

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Formaldehyde Approved, Vet_approved Pharma 95
Oxygen Approved, Vet_approved Pharma 0
Succinic acid Approved Nutra Full agonist, Agonist 0
TC-E 5002 Pharma 0
Daminozide Pharma KDM2A inhibitor 7

(1) Additional Compounds for PHF8 Gene - From: HMDB

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
Oxoglutaric acid
  • 2-Ketoglutarate
  • 2-Ketoglutaric acid
  • 2-Oxo-1,5-pentanedioate
  • 2-Oxo-1,5-pentanedioic acid
  • 2-Oxoglutarate
328-50-7

(1) ApexBio Compounds for PHF8 Gene

Compound Action Cas Number
TC-E 5002 1453071-47-0
genes like me logo Genes that share compounds with PHF8: view

Drug Products

Transcripts for PHF8 Gene

Unigene Clusters for PHF8 Gene

PHD finger protein 8:
Representative Sequences:

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for PHF8 Gene

ExUns: 1 ^ 2a · 2b · 2c ^ 3 ^ 4a · 4b ^ 5 ^ 6 ^ 7a · 7b ^ 8 ^ 9a · 9b · 9c ^ 10 ^ 11 ^ 12 ^ 13a · 13b ^ 14 ^ 15 ^ 16a · 16b ^ 17a · 17b ·
SP1: - - - - - -
SP2: - - -
SP3: - -
SP4: - - -
SP5: - -
SP6:
SP7: - -
SP8:
SP9:
SP10:
SP11:
SP12:

ExUns: 17c ^ 18 ^ 19a · 19b · 19c ^ 20 ^ 21 ^ 22 ^ 23a · 23b ^ 24a · 24b ^ 25a · 25b · 25c · 25d ^ 26a · 26b ^ 27a · 27b · 27c
SP1: - - - -
SP2: - - - -
SP3: - - -
SP4: - -
SP5: - -
SP6:
SP7:
SP8: - -
SP9: -
SP10: - -
SP11:
SP12:

Relevant External Links for PHF8 Gene

GeneLoc Exon Structure for
PHF8
ECgene alternative splicing isoforms for
PHF8

Expression for PHF8 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for PHF8 Gene

Protein differential expression in normal tissues from HIPED for PHF8 Gene

This gene is overexpressed in Lung (16.4), Testis (13.4), and Plasma (7.2).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, MaxQB, and MOPED for PHF8 Gene



Protein tissue co-expression partners for PHF8 Gene

- Elite partner

NURSA nuclear receptor signaling pathways regulating expression of PHF8 Gene:

PHF8

SOURCE GeneReport for Unigene cluster for PHF8 Gene:

Hs.133352

Evidence on tissue expression from TISSUES for PHF8 Gene

  • Nervous system(4.3)

Phenotype-based relationships between genes and organs from Gene ORGANizer for PHF8 Gene

Germ Layers:
  • ectoderm
  • mesoderm
Systems:
  • digestive
  • integumentary
  • nervous
  • reproductive
  • skeleton
Organs:
Head and neck:
  • brain
  • cheek
  • chin
  • face
  • head
  • jaw
  • lip
  • mandible
  • maxilla
  • mouth
  • nose
  • skull
Pelvis:
  • testicle
Limb:
  • digit
  • finger
  • hand
  • upper limb
General:
  • skin
genes like me logo Genes that share expression patterns with PHF8: view

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues and mRNA Expression by UniProt/SwissProt for PHF8 Gene

Orthologs for PHF8 Gene

This gene was present in the common ancestor of animals and fungi.

Orthologs for PHF8 Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia PHF8 33 34
  • 99.88 (n)
dog
(Canis familiaris)
Mammalia PHF8 33 34
  • 93.52 (n)
cow
(Bos Taurus)
Mammalia PHF8 33 34
  • 93.33 (n)
rat
(Rattus norvegicus)
Mammalia Phf8 33
  • 90.97 (n)
mouse
(Mus musculus)
Mammalia Phf8 16 34 33
  • 90.84 (n)
4921501E09Rik 34
  • 67 (a)
OneToMany
oppossum
(Monodelphis domestica)
Mammalia PHF8 34
  • 72 (a)
OneToOne
platypus
(Ornithorhynchus anatinus)
Mammalia PHF8 34
  • 71 (a)
OneToOne
lizard
(Anolis carolinensis)
Reptilia PHF8 34
  • 72 (a)
OneToOne
tropical clawed frog
(Silurana tropicalis)
Amphibia phf8 33
  • 67.28 (n)
Str.10718 33
African clawed frog
(Xenopus laevis)
Amphibia LOC398683 33
zebrafish
(Danio rerio)
Actinopterygii phf8 33 34
  • 64.65 (n)
rainbow trout
(Oncorhynchus mykiss)
Actinopterygii Omy.3567 33
worm
(Caenorhabditis elegans)
Secernentea jmjd-1.1 34
  • 27 (a)
ManyToMany
jmjd-1.2 34
  • 20 (a)
ManyToMany
baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes JHD1 34
  • 29 (a)
OneToMany
Species where no ortholog for PHF8 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • chicken (Gallus gallus)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • fruit fly (Drosophila melanogaster)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for PHF8 Gene

ENSEMBL:
Gene Tree for PHF8 (if available)
TreeFam:
Gene Tree for PHF8 (if available)

Paralogs for PHF8 Gene

Paralogs for PHF8 Gene

genes like me logo Genes that share paralogs with PHF8: view

Variants for PHF8 Gene

Sequence variations from dbSNP and Humsavar for PHF8 Gene

SNP ID Clin Chr 0X pos Sequence Context AA Info Type
rs121918524 Pathogenic, Mental retardation, X-linked, syndromic, Siderius type (MRXSSD) [MIM:300263] 54,011,232(-) TCTCT(C/T)TGAGT reference, missense
rs1057518729 Pathogenic 54,017,738(-) CATCC(-/T)GGTCC reference, frameshift-variant
rs121918522 Pathogenic 54,014,529(-) TTGTT(C/T)GAAAG reference, stop-gained
rs121918523 Pathogenic 54,016,662(-) TTGTG(A/T)AATAC reference, stop-gained
rs878853148 Pathogenic 54,002,150(-) GGTAT(C/G)GAGCC intron-variant

Structural Variations from Database of Genomic Variants (DGV) for PHF8 Gene

Variant ID Type Subtype PubMed ID
nsv524220 CNV gain 19592680
nsv435891 CNV deletion 17901297
esv3576882 CNV gain 25503493
esv3573978 CNV loss 25503493
esv3573977 CNV loss 25503493
esv2740175 CNV deletion 23290073
esv2675498 CNV deletion 23128226

Variation tolerance for PHF8 Gene

Residual Variation Intolerance Score: 3.4% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 0.99; 20.41% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for PHF8 Gene

Human Gene Mutation Database (HGMD)
PHF8
SNPedia medical, phenotypic, and genealogical associations of SNPs for
PHF8

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for PHF8 Gene

Disorders for PHF8 Gene

MalaCards: The human disease database

(7) MalaCards diseases for PHF8 Gene - From: HGMD, OMIM, ClinVar, Orphanet, Swiss-Prot, DISEASES, and GeneCards

- elite association - COSMIC cancer census association via MalaCards
Search PHF8 in MalaCards View complete list of genes associated with diseases

UniProtKB/Swiss-Prot

PHF8_HUMAN
  • Mental retardation, X-linked, syndromic, Siderius type (MRXSSD) [MIM:300263]: A syndrome characterized by mild to borderline mental retardation with or without cleft lip/cleft palate. {ECO:0000269 PubMed:16199551, ECO:0000269 PubMed:17661819, ECO:0000269 PubMed:20101266, ECO:0000269 PubMed:20208542, ECO:0000269 PubMed:20346720, ECO:0000269 PubMed:20421419, ECO:0000269 PubMed:20548336, ECO:0000269 PubMed:20622853, ECO:0000269 PubMed:20622854}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Relevant External Links for PHF8

Genetic Association Database (GAD)
PHF8
Human Genome Epidemiology (HuGE) Navigator
PHF8
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
PHF8
genes like me logo Genes that share disorders with PHF8: view

No data available for Genatlas for PHF8 Gene

Publications for PHF8 Gene

  1. Enzymatic and structural insights for substrate specificity of a family of jumonji histone lysine demethylases. (PMID: 20023638) Horton JR … Cheng X (Nature structural & molecular biology 2010) 2 3 4 60
  2. Crystal structure of the PHF8 Jumonji domain, an Nepsilon-methyl lysine demethylase. (PMID: 20067792) Yue WW … McDonough MA (FEBS letters 2010) 3 4 22 60
  3. PHF8 activates transcription of rRNA genes through H3K4me3 binding and H3K9me1/2 demethylation. (PMID: 20208542) Feng W … Grummt I (Nature structural & molecular biology 2010) 3 4 22 60
  4. Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate. (PMID: 17661819) Koivisto AM … Järvelä I (Clinical genetics 2007) 3 4 22 60
  5. Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate. (PMID: 16199551) Laumonnier F … Briault S (Journal of medical genetics 2005) 3 4 22 60

Products for PHF8 Gene

Sources for PHF8 Gene

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