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Aliases for DISC1FP1 Gene

Subcategory (RNA class) for DISC1FP1 Gene

non-coding RNA

Quality Score for this RNA gene is

3

Aliases for DISC1FP1 Gene

  • DISC1 Fusion Partner 1 (Non-Protein Coding) 2 3 5
  • DISC1/FP1 Fusion 3
  • Boymaw 3

External Ids for DISC1FP1 Gene

Previous GeneCards Identifiers for DISC1FP1 Gene

  • GC00U934060
  • GC11P089985

Summaries for DISC1FP1 Gene

GeneCards Summary for DISC1FP1 Gene

DISC1FP1 (DISC1 Fusion Partner 1 (Non-Protein Coding)) is an RNA Gene, and is affiliated with the non-coding RNA class.

No data available for Entrez Gene Summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for DISC1FP1 Gene

Genomics for DISC1FP1 Gene

Regulatory Elements for DISC1FP1 Gene

Enhancers for DISC1FP1 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
- Elite enhancer/Elite enhancer-gene association

Enhancers around DISC1FP1 on UCSC Golden Path with GeneCards custom track

Genomic Location for DISC1FP1 Gene

Chromosome:
11
Start:
90,251,232 bp from pter
End:
90,915,052 bp from pter
Size:
663,821 bases
Orientation:
Plus strand

Genomic View for DISC1FP1 Gene

Genes around DISC1FP1 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
DISC1FP1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for DISC1FP1 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for DISC1FP1 Gene

Proteins for DISC1FP1 Gene

Post-translational modifications for DISC1FP1 Gene

No Post-translational modifications

No data available for DME Specific Peptides for DISC1FP1 Gene

Domains & Families for DISC1FP1 Gene

Graphical View of Domain Structure for InterPro Entry

No data available for Gene Families , Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for DISC1FP1 Gene

Function for DISC1FP1 Gene

Animal Model Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for DISC1FP1 Gene

Localization for DISC1FP1 Gene

Subcellular locations from

COMPARTMENTS
Jensen Localization Image for DISC1FP1 Gene COMPARTMENTS Subcellular localization image for DISC1FP1 gene
Compartment Confidence
mitochondrion 1

No data available for Subcellular locations from UniProtKB/Swiss-Prot and Gene Ontology (GO) - Cellular Components for DISC1FP1 Gene

Pathways & Interactions for DISC1FP1 Gene

SuperPathways for DISC1FP1 Gene

No Data Available

Interacting Proteins for DISC1FP1 Gene

Gene Ontology (GO) - Biological Process for DISC1FP1 Gene

None

No data available for Pathways by source and SIGNOR curated interactions for DISC1FP1 Gene

Drugs & Compounds for DISC1FP1 Gene

No Compound Related Data Available

Transcripts for DISC1FP1 Gene

mRNA/cDNA for DISC1FP1 Gene

(5) Ensembl transcripts including schematic representations, and UCSC links where relevant :

Alternative Splicing Database (ASD) splice patterns (SP) for DISC1FP1 Gene

No ASD Table

Relevant External Links for DISC1FP1 Gene

GeneLoc Exon Structure for
DISC1FP1
ECgene alternative splicing isoforms for
DISC1FP1

Expression for DISC1FP1 Gene

mRNA expression in normal human tissues for DISC1FP1 Gene

mRNA differential expression in normal tissues according to GTEx for DISC1FP1 Gene

This gene is overexpressed in Spleen (x4.0).

NURSA nuclear receptor signaling pathways regulating expression of DISC1FP1 Gene:

DISC1FP1
genes like me logo Genes that share expression patterns with DISC1FP1: view

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners and mRNA Expression by UniProt/SwissProt for DISC1FP1 Gene

Orthologs for DISC1FP1 Gene

Evolution for DISC1FP1 Gene

ENSEMBL:
Gene Tree for DISC1FP1 (if available)
TreeFam:
Gene Tree for DISC1FP1 (if available)

No data available for Orthologs for DISC1FP1 Gene

Paralogs for DISC1FP1 Gene

No data available for Paralogs for DISC1FP1 Gene

Variants for DISC1FP1 Gene

Sequence variations from dbSNP and Humsavar for DISC1FP1 Gene

SNP ID Clin Chr 11 pos Sequence Context AA Info Type
rs1006133 -- 90,705,435(-) AATTT(A/G)TAGGG intron-variant
rs1112569 -- 90,815,656(-) ATGAG(A/G)TCTCA intron-variant
rs1150319 -- 90,396,047(+) AAAAT(A/G)TTTTC intron-variant
rs1150322 -- 90,515,611(+) aagga(A/G)taaga intron-variant
rs1192538 -- 90,600,211(+) AACAT(A/G)TAAAC intron-variant

Structural Variations from Database of Genomic Variants (DGV) for DISC1FP1 Gene

Variant ID Type Subtype PubMed ID
dgv1251n100 CNV loss 25217958
dgv2083n54 CNV gain 21841781
dgv2084n54 CNV loss 21841781
dgv2085n54 CNV loss 21841781
dgv2086n54 CNV loss 21841781
dgv2087n54 CNV loss 21841781
dgv2088n54 CNV loss 21841781
dgv2089n54 CNV loss 21841781
dgv2090n54 CNV loss 21841781
dgv2091n54 CNV loss 21841781
dgv2092n54 CNV loss 21841781
dgv219e214 CNV loss 21293372
dgv220e214 CNV gain 21293372
dgv221e214 CNV loss 21293372
dgv231e199 CNV deletion 23128226
dgv232e199 CNV deletion 23128226
dgv689n106 CNV deletion 24896259
esv1334387 CNV insertion 17803354
esv2106154 CNV deletion 18987734
esv21972 CNV loss 19812545
esv23063 CNV loss 19812545
esv2421664 CNV deletion 20811451
esv2496133 CNV loss 19546169
esv2505197 CNV deletion 19546169
esv2567998 CNV deletion 19546169
esv2671190 CNV deletion 23128226
esv2673272 CNV deletion 23128226
esv2673657 CNV deletion 23128226
esv2675552 CNV deletion 23128226
esv2676278 CNV deletion 23128226
esv2744884 CNV deletion 23290073
esv2744886 CNV deletion 23290073
esv2744887 CNV deletion 23290073
esv2744888 CNV deletion 23290073
esv2744889 CNV deletion 23290073
esv2744890 CNV deletion 23290073
esv2744891 CNV deletion 23290073
esv2759850 CNV gain 17122850
esv3304038 CNV mobile element insertion 20981092
esv3308593 CNV mobile element insertion 20981092
esv3384306 CNV insertion 20981092
esv3385903 CNV insertion 20981092
esv3412695 CNV insertion 20981092
esv3416315 CNV insertion 20981092
esv3548129 CNV deletion 23714750
esv3548130 CNV deletion 23714750
esv3548134 CNV deletion 23714750
esv3579841 CNV loss 25503493
esv3579842 CNV loss 25503493
esv3579993 CNV gain 25503493
esv3627198 CNV gain 21293372
esv3627200 CNV loss 21293372
esv3627201 CNV loss 21293372
esv3627204 CNV loss 21293372
esv3627206 CNV loss 21293372
esv3627207 CNV loss 21293372
esv3627208 CNV gain 21293372
esv3627209 CNV loss 21293372
esv3627210 CNV loss 21293372
esv3627212 CNV loss 21293372
esv3627213 CNV loss 21293372
esv3627215 CNV loss 21293372
esv3627216 CNV loss 21293372
esv3627221 CNV loss 21293372
esv3627222 CNV loss 21293372
esv3627225 CNV gain 21293372
esv3627226 CNV loss 21293372
esv3892061 CNV loss 25118596
esv3892062 CNV loss 25118596
esv3892063 CNV loss 25118596
esv4120 CNV loss 18987735
esv5366 CNV loss 18987735
esv8934 CNV loss 19470904
nsv1035213 CNV gain 25217958
nsv1039065 CNV gain 25217958
nsv1046353 CNV loss 25217958
nsv1046366 CNV gain 25217958
nsv1047116 CNV loss 25217958
nsv1048624 CNV loss 25217958
nsv1053196 CNV loss 25217958
nsv1053917 CNV gain 25217958
nsv1070979 CNV deletion 25765185
nsv1119900 CNV deletion 24896259
nsv1129324 OTHER inversion 24896259
nsv1138062 CNV deletion 24896259
nsv1139557 CNV duplication 24896259
nsv1159915 CNV duplication 26073780
nsv427 CNV insertion 18451855
nsv428 CNV insertion 18451855
nsv442625 CNV loss 18776908
nsv468788 CNV loss 19166990
nsv474506 CNV novel sequence insertion 20440878
nsv476392 CNV novel sequence insertion 20440878
nsv476402 CNV novel sequence insertion 20440878
nsv479220 CNV novel sequence insertion 20440878
nsv479246 CNV novel sequence insertion 20440878
nsv480338 CNV novel sequence insertion 20440878
nsv510267 OTHER sequence alteration 20534489
nsv514638 CNV loss 21397061
nsv519936 CNV loss 19592680
nsv521151 CNV loss 19592680
nsv555832 CNV gain 21841781
nsv555833 CNV loss 21841781
nsv555836 CNV loss 21841781
nsv555837 CNV loss 21841781
nsv555838 CNV loss 21841781
nsv555843 CNV loss 21841781
nsv555871 CNV loss 21841781
nsv555880 CNV loss 21841781
nsv555881 CNV loss 21841781
nsv555882 CNV loss 21841781
nsv555883 CNV loss 21841781
nsv555884 CNV loss 21841781
nsv555886 CNV loss 21841781
nsv555888 CNV loss 21841781
nsv818856 CNV gain 17921354
nsv818857 CNV gain 17921354
nsv826029 CNV loss 20364138
nsv957386 CNV deletion 24416366
nsv975966 CNV duplication 23825009
nsv976514 CNV deletion 23825009

Relevant External Links for DISC1FP1 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for
DISC1FP1

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot and Variation tolerance for DISC1FP1 Gene

Disorders for DISC1FP1 Gene

Relevant External Links for DISC1FP1

Atlas of Genetics and Cytogenetics in Oncology and Haematology:
DISC1FP1

No disorders were found for DISC1FP1 Gene.

No data available for MalaCards , UniProtKB/Swiss-Prot and Genatlas for DISC1FP1 Gene

Publications for DISC1FP1 Gene

  1. Boymaw, overexpressed in brains with major psychiatric disorders, may encode a small protein to inhibit mitochondrial function and protein translation. (PMID: 25943690) Ji B. … Zhou X. (Am. J. Med. Genet. B Neuropsychiatr. Genet. 2015) 3 65
  2. Inhibition of protein translation by the DISC1-Boymaw fusion gene from a Scottish family with major psychiatric disorders. (PMID: 24908665) Ji B. … Zhou X. (Hum. Mol. Genet. 2014) 3 65
  3. A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus. (PMID: 25130324) Cai D.C. … Hagoort P. (Genes Brain Behav. 2014) 3 65
  4. A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins. (PMID: 22547224) Eykelenboom J.E. … Millar J.K. (Hum. Mol. Genet. 2012) 3 65
  5. Full-length transcriptome analysis of human retina-derived cell lines ARPE-19 and Y79 using the vector-capping method. (PMID: 21697133) Oshikawa M. … Kato S. (Invest. Ophthalmol. Vis. Sci. 2011) 3 65

Products for DISC1FP1 Gene

Sources for DISC1FP1 Gene

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