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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

ST13P4 Gene

pseudogene   GIFtS: 33
GCID: GC13P050747

suppression of tumorigenicity 13 (colon carcinoma) (Hsp7...

(Previous names: family with sequence similarity 10, member A4 pseudogene...)
(Previous symbol: FAM10A4)
 Explore 11 diseases affiliated with
ST13P4 via our new
 Human Malady Compendium 
Biological research products
for ST13P4
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

This gene clusters with an RNA gene
Subcategory (RNA class): lncRNA

Quality score for the ORGUL clustered with this gene is 3

Aliases
Suppression Of Tumorigenicity 13 (Colon Carcinoma) (Hsp70 Interacting
Protein) Pseudogene 41 2
FAM10A41 2 3
FAM10A4P1 2
Family With Sequence Similarity 10, Member A4 Pseudogene1
Suppression Of Tumorigenicity 13 Pseudogene 43

External Ids:    HGNC: 184871   Entrez Gene: 1451652   Ensembl: ENSG000002321507   UniProtKB: Q8IZP23   
ORGUL members:         
NONCODE:n405439    

Export aliases for ST13P4 gene to outside databases

Previous GC identifer: GC13P031541


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

  --

(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000013.10  NC_018924.1  NT_024524.14  
Regulatory elements:
   Search SABiosciences Regulatory transcription factor binding sites for ST13P4
         Other transcription factors

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Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat ST13P4


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 13q14.3   Ensembl cytogenetic band:  13q14.2   HGNC cytogenetic band: 13q14

ST13P4 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
ST13P4 gene location

GeneLoc information about chromosome 13         GeneLoc Exon Structure

GeneLoc location for GC13P050747:  view genomic region     (about GC identifiers)

Start:
50,746,154 bp from pter      End:
50,747,752 bp from pter
Size:
1,599 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: ST134_HUMAN, Q8IZP2 (See protein sequence)
Recommended Name: Putative protein FAM10A4  
Size: 240 amino acids; 27407 Da
Subcellular location: Cytoplasm (Probable)
Caution: Could be the product of a pseudogene

Explore the universe of human proteins at neXtProt for ST13P4: NX_Q8IZP2

ST13P4 Protein expression data from MOPED and PaxDb: --

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Gene Ontology (GO): 1 cellular component term (GO ID links to tree view):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0005737cytoplasm IEA--


ST13P4 for ontologies           About GeneDecksing



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(According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
About This Section

ST13P4 for domains           About GeneDecksing

4 InterPro domains/families:
 IPR011990 TPR-like_helical
 IPR013105 TPR_2
 IPR013026 TPR-contain_dom
 IPR019734 TPR_repeat

Graphical View of Domain Structure for InterPro Entry Q8IZP2

ProtoNet protein and cluster: Q8IZP2

UniProtKB/Swiss-Prot: ST134_HUMAN, Q8IZP2
Similarity: Belongs to the FAM10 family
Similarity: Contains 3 TPR repeats


(According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
About This Section

miRNA
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1 GenomeRNAi human phenotype for ST13P4:
 Decreased Wnt reporter activit 


(Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
About This Section



Interactions:

    Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for ST13P4

1 Interacting protein for ST13P4 (Q8IZP22, 3) via UniProtKB, MINT, STRING, and/or I2D
InteractantInteraction Details
GeneCardExternal ID(s)
MAP3K3Q997592, 3MINT-48499 I2D: score=2 
About this table

(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
About This Section
Browse Small Molecules at EMD Millipore
Browse drugs & compounds from Enzo Life Sciences

Browse Tocris compounds for ST13P4
Search CenterWatch for drugs/clinical trials and news about ST13P4 

(Secondary structures according to fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
RefSeq according to Entrez Gene,
DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
RNAi Products from EMD Millipore,
siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
About This Section

REFSEQ mRNAs for ST13P4 gene: 
NM_153290.1  

Unigene Cluster for ST13P4:

Suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) pseudogene 4
Hs.511834  [show with all ESTs]
Unigene Representative Sequence: AF539468
1 Ensembl transcript including schematic representation, and UCSC links where relevant:
ENST00000495613(uc001vej.3)

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Inhib. RNA
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Additional cDNA sequence: 

AF539468.1 NR_002183.1 

12 DOTS entries:

DT.100000399  DT.100892017  DT.456282  DT.120774954  DT.99998054  DT.100034556  DT.100892030  DT.100892026 
DT.100678206  DT.100757889  DT.100892025  DT.100892042 

7 AceView cDNA sequences:

NM_153290 AF539468 AI929839 BF089934 AW604071 CD579790 BX407161 

GeneLoc Exon Structure


(RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section

ST13P4 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: --

Microarray
RNAseq (Illumina Body Map)
(100×FPKM)½
SAGE (Serial Analysis of Gene Expression)

About this image
SOURCE GeneReport for Unigene cluster: Hs.511834

UniProtKB/Swiss-Prot: ST134_HUMAN, Q8IZP2
Tissue specificity: Highly expressed in bone marrow and weakly in placenta, pancreas, heart and HeLa cell line

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In Situ
Assay Products:
 

 
Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for ST13P4

(Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
About This Section

This gene was present in the common ancestor of chordates.

Orthologs for ST13P4 gene from 1 species (see representative species )    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
tropical clawed frog
(Xenopus tropicalis)
Amphibia Str.21232 Transcribed sequence with weak similarity to protein more 77.91(n)    AL775197.2 
        Species with no ortholog for ST13P4

ENSEMBL Gene Tree for ST13P4 (if available)
TreeFam Gene Tree for ST13P4 (if available) 

(Paralogs according to 1HomoloGene,
2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
About This Section
  --

(SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section

10/54 NCBI SNPs in ST13P4 are shown (see all 54    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 13 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs773461481,2
C,--50744245(+) ATACAA/GTGTGT 1 -- us2k12Minor allele frequency- G:0.03WA 120
rs740765621,2
C,--50744605(+) CAGCAC/GTTGTC 1 -- us2k13Minor allele frequency- G:0.03WA EA 240
rs7905341,2
C,F,O,A,H,--50744791(+) AAATAC/GTGTAA 1 -- us2k117Minor allele frequency- N:0.00NS EA NA WA CSA 1004
rs1889730271,2
--50744890(+) CTAAGA/CAAGGA 1 -- us2k10--------
rs1817275541,2
--50745016(+) CATAGA/GAGTCA 1 -- us2k10--------
rs1875063091,2
--50745022(+) AGTCAC/TAAAAG 1 -- us2k10--------
rs20666111,2
C,H,--50745062(+) GAGCCG/AACATG 1 -- us2k14Minor allele frequency- A:0.00NS EA 418
rs20666121,2
C,F,A,H,--50745395(+) TAATCG/AGCCGG 1 -- us2k117Minor allele frequency- A:0.37NS EA NA WA 2120
rs1906515001,2
--50745399(+) CGGCCC/GGGCGC 1 -- us2k10--------
rs1827727741,2
--50745589(+) AGAATC/GGCTTG 1 -- us2k10--------

HapMap Linkage Disequilibrium report for ST13P4 (50746154 - 50747752 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
      Database of Genomic Variants (DGV) variations for ST13P4: --

SABiosciences Cancer Mutation PCR Assays
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(in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
About This Section

ST13P4 for disorders           About GeneDecksing

11 diseases for ST13P4:    About MalaCards
colon carcinoma    carcinoma    chronic lymphocytic leukemia    lymphocytic leukemia
celiac disease    multiple myeloma    myeloma    leukemia
t-cell leukemia    prostate cancer    prostatitis


Export disorders for ST13P4 gene to outside databases

(in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
About This Section

PubMed articles for ST13P4 gene integrated from 9 sources:
(articles sorted by number of sources associating them with ST13P4)
    Utopia: connect your pdf to the dynamic
world of online information

  1. Characterization of FAM10A4, a member of the ST13 tumor suppressor gene family that maps to the 13q14.3 region associated with B-Cell leukemia, multiple myeloma, and prostate cancer. (PubMed id 12079276)1, 2 Sossey-Alaoui K.... Cowell J.K. (2002)
  2. The proteomic analysis of endogenous FAT10 substrates identifies p62/SQSTM1 as a substrate of FAT10ylation. (PubMed id 22797925)1 Aichem A....Groettrup M. (2012)
  3. Systematic and quantitative assessment of the ubiquiti n-modified proteome. (PubMed id 21906983)1 Kim W....Gygi S.P. (2011)
  4. Multiple common variants for celiac disease influenci ng immune gene expression. (PubMed id 20190752)1 Dubois P.C....van Heel D.A. (2010)
  5. Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. (PubMed id 17081983)1 Olsen J.V....Mann M. (2006)
  6. Phosphoproteomic analysis of the human pituitary. (PubMed id 16807684)1 Beranova-Giorgianni S.... Giorgianni F. (2006)
  7. The DNA sequence and analysis of human chromosome 13. (PubMed id 15057823)2 Dunham A.... Ross M.T. (2004)
  8. RFP2, c13ORF1, and FAM10A4 are the most likely tumor suppressor gene candidates for B-cell chronic lymphocytic leukemia. (PubMed id 14499696)9 van Everdink W.J.... Buys C.H. (2003)

(in PubMed, OMIM, and NCBI Bookshelf)
About This Section
 ANDOR
Aliases
Free Text  

  Query String
PubMed
OMIM
NCBI Bookshelf
  (Note: In FireFox, select the above section and copy using Ctrl-C)

(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
About This Section
Entrez Gene: 145165 HGNC: 18487 AceView: FAM10A4 Ensembl:ENSG00000232150 euGenes: HUgn145165
ECgene: ST13P4 H-InvDB: ST13P4

(According to HUGE)
About This Section
  --

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
About This Section
NameDescription
PharmGKB entry for ST13P4 Pharmacogenomics, SNPs, Pathways

(Patent information from GeneIP,
Licensable technologies from WIS Yeda, Salk, Tufts,
IP news from LifeMap Sciences, Inc.)
About This Section
Patent Information for ST13P4 gene:
Search GeneIP for patents involving ST13P4

GeneCards and IP:
Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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About This Section

 
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