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Aliases for SLX4 Gene

Aliases for SLX4 Gene

  • SLX4 Structure-Specific Endonuclease Subunit 2 3 5
  • BTB/POZ Domain-Containing Protein 12 3 4
  • BTBD12 3 4
  • SLX4 Structure-Specific Endonuclease Subunit Homolog (S. Cerevisiae) 2
  • Structure-Specific Endonuclease Subunit SLX4 3
  • Fanconi Anemia, Complementation Group P 2
  • BTB (POZ) Domain Containing 12 2
  • KIAA1784 4
  • KIAA1987 4
  • MUS312 3
  • FANCP 3

External Ids for SLX4 Gene

Previous HGNC Symbols for SLX4 Gene

  • BTBD12

Previous GeneCards Identifiers for SLX4 Gene

  • GC16M003632

Summaries for SLX4 Gene

Entrez Gene Summary for SLX4 Gene

  • This gene encodes a protein that functions as an assembly component of multiple structure-specific endonucleases. These endonuclease complexes are required for repair of specific types of DNA lesions and critical for cellular responses to replication fork failure. Mutations in this gene were found in patients with Fanconi anemia. [provided by RefSeq, Sep 2016]

GeneCards Summary for SLX4 Gene

SLX4 (SLX4 Structure-Specific Endonuclease Subunit) is a Protein Coding gene. Diseases associated with SLX4 include Fanconi Anemia, Complementation Group P and Fanconi Anemia, Complementation Group A. Among its related pathways are DNA Double-Strand Break Repair and Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA). GO annotations related to this gene include enzyme activator activity and 5-flap endonuclease activity.

UniProtKB/Swiss-Prot for SLX4 Gene

  • Regulatory subunit that interacts with and increases the activity of different structure-specific endonucleases. Has several distinct roles in protecting genome stability by resolving diverse forms of deleterious DNA structures originating from replication and recombination intermediates and from DNA damage. Component of the SLX1-SLX4 structure-specific endonuclease that resolves DNA secondary structures generated during DNA repair and recombination. Has endonuclease activity towards branched DNA substrates, introducing single-strand cuts in duplex DNA close to junctions with ss-DNA. Has a preference for 5-flap structures, and promotes symmetrical cleavage of static and migrating Holliday junctions (HJs). Resolves HJs by generating two pairs of ligatable, nicked duplex products. Interacts with the structure-specific ERCC4-ERCC1 endonuclease and promotes the cleavage of bubble structures. Interacts with the structure-specific MUS81-EME1 endonuclease and promotes the cleavage of 3-flap and replication fork-like structures. SLX4 is required for recovery from alkylation-induced DNA damage and is involved in the resolution of DNA double-strand breaks.

Additional gene information for SLX4 Gene

No data available for CIViC summary , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for SLX4 Gene

Genomics for SLX4 Gene

Regulatory Elements for SLX4 Gene

Enhancers for SLX4 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
GH16H003148 1.7 Ensembl ENCODE dbSUPER 18.2 +460.4 460413 4 MLX ZFP64 YY1 SLC30A9 ZNF143 SP3 NFYC ZC3H11A MEF2D SSRP1 CREBBP E4F1 ZNF263 THOC6 ZNF597 ZNF213-AS1 SRRM2 ZNF205 AMDHD2 ENSG00000261938
GH16H003156 1.7 FANTOM5 ENCODE dbSUPER 18.2 +452.8 452805 3 HDGF ARNT ARID4B SIN3A DMAP1 ZNF2 ZBTB7B YY1 ZNF766 ZNF207 ZNF75A ZNF213-AS1 ZNF205 E4F1 CREBBP ENSG00000261938 RNPS1 PDPK2P LOC652276 MTCO1P28
GH16H002903 1.9 FANTOM5 Ensembl ENCODE dbSUPER 9.9 +706.0 705991 3 HDGF PKNOX1 ZFP64 ARID4B SIN3A DMAP1 ZNF2 YY1 ZNF143 ZNF548 CREBBP ZNF597 ZNF263 ZNF174 ENSG00000261938 TBL3 ZNF75A TSC2 FLYWCH2 E4F1
GH16H004270 1.8 FANTOM5 ENCODE dbSUPER 9.9 -661.1 -661117 4 HDGF PKNOX1 FOXA2 MLX ARNT ZFP64 ARID4B SIN3A FEZF1 DMAP1 ZNF500 ZNF75A CREBBP ANKS3 ENSG00000261938 ZNF597 ZNF174 TIGD7 ENSG00000261789 LOC105371067
GH16H002964 1.5 FANTOM5 ENCODE dbSUPER 9.9 +647.7 647670 2 PKNOX1 ARID4B SIN3A DMAP1 ZNF2 GLIS2 SP3 SP5 ZNF610 SMARCA4 ENSG00000200059 ENSG00000270168 ENSG00000261240 SLX4 MMP25 KREMEN2 LOC105371055
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around SLX4 on UCSC Golden Path with GeneCards custom track

Genomic Location for SLX4 Gene

Chromosome:
16
Start:
3,581,165 bp from pter
End:
3,611,598 bp from pter
Size:
30,434 bases
Orientation:
Minus strand

Genomic View for SLX4 Gene

Genes around SLX4 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
SLX4 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for SLX4 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for SLX4 Gene

Proteins for SLX4 Gene

  • Protein details for SLX4 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Q8IY92-SLX4_HUMAN
    Recommended name:
    Structure-specific endonuclease subunit SLX4
    Protein Accession:
    Q8IY92
    Secondary Accessions:
    • Q69YT8
    • Q8TF15
    • Q96JP1

    Protein attributes for SLX4 Gene

    Size:
    1834 amino acids
    Molecular mass:
    200012 Da
    Quaternary structure:
    • Forms a heterodimer with SLX1A/GIYD1. Interacts with ERCC4; catalytic subunit of the ERCC4-ERCC1 endonuclease. Interacts with MUS81; catalytic subunit of the MUS81-EME1 endonuclease. Interacts with MSH2; component of the MSH2-MSH3 mismatch repair complex. Interacts with TERF2-TERF2IP. Interacts with PLK1 and SLX4IP.

    Three dimensional structures from OCA and Proteopedia for SLX4 Gene

    Alternative splice isoforms for SLX4 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for SLX4 Gene

Post-translational modifications for SLX4 Gene

  • Modification sites at PhosphoSitePlus
  • Modification sites at neXtProt

Other Protein References for SLX4 Gene

ENSEMBL proteins:
REFSEQ proteins:

No data available for DME Specific Peptides for SLX4 Gene

Domains & Families for SLX4 Gene

Gene Families for SLX4 Gene

HGNC:
Human Protein Atlas (HPA):
  • Disease related genes
  • Predicted intracellular proteins

Protein Domains for SLX4 Gene

Suggested Antigen Peptide Sequences for SLX4 Gene

GenScript: Design optimal peptide antigens:

Graphical View of Domain Structure for InterPro Entry

Q8IY92

UniProtKB/Swiss-Prot:

SLX4_HUMAN :
  • Belongs to the SLX4 family.
Family:
  • Belongs to the SLX4 family.
genes like me logo Genes that share domains with SLX4: view

Function for SLX4 Gene

Molecular function for SLX4 Gene

UniProtKB/Swiss-Prot Function:
Regulatory subunit that interacts with and increases the activity of different structure-specific endonucleases. Has several distinct roles in protecting genome stability by resolving diverse forms of deleterious DNA structures originating from replication and recombination intermediates and from DNA damage. Component of the SLX1-SLX4 structure-specific endonuclease that resolves DNA secondary structures generated during DNA repair and recombination. Has endonuclease activity towards branched DNA substrates, introducing single-strand cuts in duplex DNA close to junctions with ss-DNA. Has a preference for 5-flap structures, and promotes symmetrical cleavage of static and migrating Holliday junctions (HJs). Resolves HJs by generating two pairs of ligatable, nicked duplex products. Interacts with the structure-specific ERCC4-ERCC1 endonuclease and promotes the cleavage of bubble structures. Interacts with the structure-specific MUS81-EME1 endonuclease and promotes the cleavage of 3-flap and replication fork-like structures. SLX4 is required for recovery from alkylation-induced DNA damage and is involved in the resolution of DNA double-strand breaks.

Gene Ontology (GO) - Molecular Function for SLX4 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0004520 endodeoxyribonuclease activity TAS --
GO:0005515 protein binding IPI 19595721
GO:0008047 enzyme activator activity IDA 19596235
GO:0008821 contributes_to crossover junction endodeoxyribonuclease activity IDA 19595721
GO:0017108 contributes_to 5-flap endonuclease activity IDA,IEA 19595721
genes like me logo Genes that share ontologies with SLX4: view
genes like me logo Genes that share phenotypes with SLX4: view

Human Phenotype Ontology for SLX4 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for SLX4 Gene

MGI Knock Outs for SLX4:

Animal Model Products

CRISPR Products

Inhibitory RNA Products

Clone Products

  • Addgene plasmids for SLX4
  • Applied Biological Materials Clones for SLX4
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

No data available for Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog , Transcription Factor Targets and HOMER Transcription for SLX4 Gene

Localization for SLX4 Gene

Subcellular locations from UniProtKB/Swiss-Prot for SLX4 Gene

Nucleus. Note=Localizes to sites of DNA damage.

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 SLX4 gene
Compartment Confidence
nucleus 5
cytosol 5

Subcellular locations from the

Human Protein Atlas (HPA)
  • Cell Junctions (3)
  • Cytosol (3)
  • Nucleoplasm (3)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for SLX4 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000781 chromosome, telomeric region IDA 24012755
GO:0000784 colocalizes_with nuclear chromosome, telomeric region IDA 19596235
GO:0000790 colocalizes_with nuclear chromatin IDA 19596235
GO:0005634 nucleus IEA --
GO:0005654 nucleoplasm TAS --
genes like me logo Genes that share ontologies with SLX4: view

Pathways & Interactions for SLX4 Gene

genes like me logo Genes that share pathways with SLX4: view

SIGNOR curated interactions for SLX4 Gene

Activates:

Gene Ontology (GO) - Biological Process for SLX4 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000706 meiotic DNA double-strand break processing IBA --
GO:0000712 resolution of meiotic recombination intermediates IBA --
GO:0000724 double-strand break repair via homologous recombination IMP 19595721
GO:0006260 DNA replication IEA --
GO:0006281 DNA repair IMP 19595722
genes like me logo Genes that share ontologies with SLX4: view

Drugs & Compounds for SLX4 Gene

No Compound Related Data Available

Transcripts for SLX4 Gene

Unigene Clusters for SLX4 Gene

SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae):
Representative Sequences:

CRISPR Products

Inhibitory RNA Products

Clone Products

  • Addgene plasmids for SLX4
  • Applied Biological Materials Clones for SLX4
  • Vectors and viruses for ORF, Lenti, Retro, Adenovirus, AAV, and more

Alternative Splicing Database (ASD) splice patterns (SP) for SLX4 Gene

No ASD Table

Relevant External Links for SLX4 Gene

GeneLoc Exon Structure for
SLX4
ECgene alternative splicing isoforms for
SLX4

Expression for SLX4 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for SLX4 Gene

mRNA differential expression in normal tissues according to GTEx for SLX4 Gene

This gene is overexpressed in Brain - Cerebellum (x4.3).

Protein differential expression in normal tissues from HIPED for SLX4 Gene

This gene is overexpressed in Nasal epithelium (51.6) and Cervix (12.7).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, MaxQB, and MOPED for SLX4 Gene



NURSA nuclear receptor signaling pathways regulating expression of SLX4 Gene:

SLX4

SOURCE GeneReport for Unigene cluster for SLX4 Gene:

Hs.143681

Evidence on tissue expression from TISSUES for SLX4 Gene

  • Nervous system(4.2)
  • Liver(4.1)

Phenotype-based relationships between genes and organs from Gene ORGANizer for SLX4 Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
Systems:
  • cardiovascular
  • digestive
  • endocrine
  • immune
  • integumentary
  • lymphatic
  • nervous
  • reproductive
  • respiratory
  • skeletal muscle
  • skeleton
  • urinary
Organs:
Head and neck:
  • brain
  • cerebellum
  • cranial nerve
  • ear
  • eye
  • eyelid
  • face
  • head
  • neck
  • nose
  • outer ear
  • pituitary gland
  • skull
Thorax:
  • breast
  • esophagus
  • heart
  • lung
  • rib
  • rib cage
Abdomen:
  • intestine
  • kidney
  • large intestine
  • liver
  • stomach
Pelvis:
  • anus
  • ovary
  • pelvis
  • penis
  • prostate
  • rectum
  • testicle
  • ureter
  • uterus
  • vagina
  • vulva
Limb:
  • arm
  • digit
  • finger
  • forearm
  • hand
  • radius
  • upper limb
General:
  • blood
  • blood vessel
  • bone marrow
  • coagulation system
  • hair
  • peripheral nervous system
  • red blood cell
  • skin
  • spinal column
  • vertebrae
  • white blood cell
genes like me logo Genes that share expression patterns with SLX4: view

Primer Products

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , Protein tissue co-expression partners and mRNA Expression by UniProt/SwissProt for SLX4 Gene

Orthologs for SLX4 Gene

This gene was present in the common ancestor of chordates.

Orthologs for SLX4 Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia SLX4 33 34
  • 99.04 (n)
dog
(Canis familiaris)
Mammalia SLX4 33 34
  • 74.36 (n)
cow
(Bos Taurus)
Mammalia SLX4 33 34
  • 73.2 (n)
rat
(Rattus norvegicus)
Mammalia Slx4 33
  • 71.11 (n)
mouse
(Mus musculus)
Mammalia Slx4 33 16 34
  • 70.59 (n)
platypus
(Ornithorhynchus anatinus)
Mammalia SLX4 34
  • 50 (a)
OneToOne
oppossum
(Monodelphis domestica)
Mammalia SLX4 34
  • 45 (a)
OneToOne
chicken
(Gallus gallus)
Aves SLX4 33 34
  • 52.58 (n)
lizard
(Anolis carolinensis)
Reptilia SLX4 34
  • 52 (a)
OneToOne
tropical clawed frog
(Silurana tropicalis)
Amphibia Str.16284 33
zebrafish
(Danio rerio)
Actinopterygii SLX4 (2 of 2) 34
  • 42 (a)
OneToMany
slx4 34
  • 26 (a)
OneToMany
Species where no ortholog for SLX4 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • 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)
  • rainbow trout (Oncorhynchus mykiss)
  • 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)
  • worm (Caenorhabditis elegans)

Evolution for SLX4 Gene

ENSEMBL:
Gene Tree for SLX4 (if available)
TreeFam:
Gene Tree for SLX4 (if available)

Paralogs for SLX4 Gene

No data available for Paralogs for SLX4 Gene

Variants for SLX4 Gene

Sequence variations from dbSNP and Humsavar for SLX4 Gene

SNP ID Clin Chr 16 pos Sequence Context AA Info Type
rs878855162 Pathogenic 3,589,909(-) CGTGA(-/GAGC)AGCCC reference, frameshift-variant
rs111738042 Likely benign 3,582,346(+) ATCAG(C/T)TCCGC reference, missense
rs112511042 Likely benign 3,600,990(+) ATGGG(C/T)GGGCT reference, synonymous-codon, utr-variant-5-prime
rs112596894 Likely benign 3,589,770(+) CGTGT(A/G/T)CTGAG reference, missense
rs113490934 Likely benign 3,600,986(+) GAACA(C/T)GGGTG reference, missense, utr-variant-5-prime

Structural Variations from Database of Genomic Variants (DGV) for SLX4 Gene

Variant ID Type Subtype PubMed ID
nsv1111122 CNV tandem duplication 24896259
nsv517451 CNV loss 19592680
nsv518509 CNV gain 19592680
nsv571255 CNV gain 21841781
nsv833128 CNV loss 17160897

Variation tolerance for SLX4 Gene

Residual Variation Intolerance Score: 98.8% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 10.53; 91.14% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for SLX4 Gene

Human Gene Mutation Database (HGMD)
SLX4
SNPedia medical, phenotypic, and genealogical associations of SNPs for
SLX4

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for SLX4 Gene

Disorders for SLX4 Gene

MalaCards: The human disease database

(6) MalaCards diseases for SLX4 Gene - From: HGMD, OMIM, ClinVar, GeneTests, Orphanet, DISEASES, and GeneCards

Disorder Aliases PubMed IDs
fanconi anemia, complementation group p
  • fanconi anemia complementation group p
fanconi anemia, complementation group a
  • fanconi's anemia
slx4-related fanconi anemia
maternal uniparental disomy of chromosome 16
  • upd(16)mat
xeroderma pigmentosum, group f
  • xeroderma pigmentosum, type f/cockayne syndrome
- elite association - COSMIC cancer census association via MalaCards
Search SLX4 in MalaCards View complete list of genes associated with diseases

UniProtKB/Swiss-Prot

SLX4_HUMAN
  • Fanconi anemia complementation group P (FANCP) [MIM:613951]: A disorder affecting all bone marrow elements and resulting in anemia, leukopenia and thrombopenia. It is associated with cardiac, renal and limb malformations, dermal pigmentary changes, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage) and defective DNA repair. Some individuals affected by Fanconi anemia of complementation group P have skeletal anomalies. {ECO:0000269 PubMed:21240275, ECO:0000269 PubMed:21240277}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Relevant External Links for SLX4

Atlas of Genetics and Cytogenetics in Oncology and Haematology:
SLX4
genes like me logo Genes that share disorders with SLX4: view

No data available for Genatlas for SLX4 Gene

Publications for SLX4 Gene

  1. Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repair. (PMID: 19595721) Muñoz IM … Rouse J (Molecular cell 2009) 2 3 4 60
  2. Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. (PMID: 11347906) Nagase T … Ohara O (DNA research : an international journal for rapid publication of reports on genes and genomes 2001) 2 3 4 60
  3. Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases. (PMID: 22911665) Bakker JL … Waisfisz Q (Human mutation 2013) 3 4 60
  4. Mutations of the SLX4 gene in Fanconi anemia. (PMID: 21240275) Kim Y … Smogorzewska A (Nature genetics 2011) 3 4 60
  5. SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. (PMID: 21240277) Stoepker C … de Winter JP (Nature genetics 2011) 3 4 60

Products for SLX4 Gene

Sources for SLX4 Gene

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