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

C11orf92 Gene

protein-coding   GIFtS: 35
GCID: GC11M111164

chromosome 11 open reading frame 92

 Explore 2 diseases affiliated with
C11orf92 via our new
 Human Malady Compendium 
Biological research products
for C11orf92
    

(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
Chromosome 11 Open Reading Frame 921 2
FLJ458031

External Ids:    HGNC: 337891   Entrez Gene: 3999482   Ensembl: ENSG000001961677   UniProtKB: Q6ZS623   
ORGUL members:         
NONCODE:n409752    

Export aliases for C11orf92 gene to outside databases

Previous GC identifers: GC11M110670 GC11M107090


(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_000011.9  NC_018922.1  NT_033899.8  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the C11orf92 gene promoter:
         c-Fos   E2F-4   E2F-3a   E2F-5   E2F-2   Nkx2-5   E2F-1   E2F   Sox9   c-Jun   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidC11orf92 promoter sequence
   Search SABiosciences Chromatin IP Primers for C11orf92

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat C11orf92


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

Entrez Gene cytogenetic band: 11q23.1   Ensembl cytogenetic band:  11q23.1   HGNC cytogenetic band: 11q23.1

C11orf92 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
C11orf92 gene location

GeneLoc information about chromosome 11         GeneLoc Exon Structure

GeneLoc location for GC11M111164:  view genomic region     (about GC identifiers)

Start:
111,164,114 bp from pter      End:
111,175,770 bp from pter
Size:
11,657 bases      Orientation:
minus 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: CK092_HUMAN, Q6ZS62 (See protein sequence)
Recommended Name: Uncharacterized protein C11orf92  
Size: 124 amino acids; 13401 Da
Subcellular location: Membrane; Single-pass membrane protein (Potential)

Explore the universe of human proteins at neXtProt for C11orf92: NX_Q6ZS62

C11orf92 Protein expression data from MOPED and PaxDb:    About this image 

Estimated protein expression log10 (pmol).


ENSEMBL proteins: 
 ENSP00000437253   ENSP00000347601   ENSP00000438980  

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Uscn Proteins for C11orf92

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

GO IDQualified GO termEvidencePubMed IDs
GO:0016021integral to membrane IEA--


C11orf92 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

ProtoNet protein and cluster: Q6ZS62


(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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(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 C11orf92

(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 C11orf92
Search CenterWatch for drugs/clinical trials and news about C11orf92 / CK092 

(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,
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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 C11orf92 gene: 
NM_207429.2  

Unigene Cluster for C11orf92:

Chromosome 11 open reading frame 92
Hs.729225  [show with all ESTs]
Unigene Representative Sequence: CR936778
4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
ENST00000532918(uc001ple.3) ENST00000355430(uc001pld.3) ENST00000526150
ENST00000540738

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Inhib. RNA
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Additional cDNA sequence: 

AB096245.1 AK127703.1 CR936778.1 NR_034154.1 

6 DOTS entries:

DT.454859  DT.105142  DT.120712119  DT.86847428  DT.97834406  DT.91961785 

24/43 AceView cDNA sequences (see all 43):

AI806340 AW573293 CB241386 NM_207429 BX486062 AW661751 CA314483 BM853126 
BF590585 AB096245 AW058265 CN478733 AK127703 BX486313 BM823942 CA437027 
CF121410 BX097686 AI200281 AI149706 BX486061 BM795014 AI985511 BG291067 

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

C11orf92 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: ATGAAAATCT

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

About this image
See C11orf92 Protein Expression from SPIRE MOPED and PaxDB
Genevestigator expression for C11orf92

SOURCE GeneReport for Unigene cluster: Hs.729225
    SABiosciences Custom PCR Arrays for C11orf92
Primer
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In Situ
Assay Products:
 

 
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(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 human and mouse.

Orthologs for C11orf92 gene from 1 species (see representative species )    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
mouse
(Mus musculus)
Mammalia 2010007H06Rik5 RIKEN cDNA 2010007H06 gene   --   9 (28.04 cM) 51280295 


ENSEMBL Gene Tree for C11orf92 (if available)
TreeFam Gene Tree for C11orf92 (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

10/72 NCBI SNPs in C11orf92 are shown (see all 72    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 11 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs1139592751,2
C,--107088626(+) TATTGA/TGGCAC 1 -- ds50010--------
rs10547681,2
C,--107089389(-) ACGTCA/CGTCTC 1 -- nc-transcript-variant5Minor allele frequency- C:0.01MN NS NA 344
rs1130597891,2
C,--107089393(+) CKGACG/ATAGCA 1 -- nc-transcript-variant1Minor allele frequency- A:0.50WA 2
rs456155361,2
C,F,--107089693(+) TACGTG/TGGGGG 1 -- nc-transcript-variant2Minor allele frequency- T:0.14NS NA 156
rs786487511,2
F,--107089813(+) GGGTAT/CGGACT 1 -- nc-transcript-variant1Minor allele frequency- C:0.03EA 120
rs455520371,2
C,F,--107090069(+) CTCACA/GATAGA 1 -- nc-transcript-variant2Minor allele frequency- G:0.02NS NA 158
rs1120422711,2
--107090098(+) TAGGAT/GAAGAG 1 -- nc-transcript-variant1Minor allele frequency- G:0.00CSA 1
rs1437870711,2
--107090170(+) CCTAGC/TGCATA 1 -- nc-transcript-variant0--------
rs770866631,2
C,--107090583(+) GTTCTA/CAGTCT 1 -- nc-transcript-variant0--------
rs762340741,2
C,F,--107090591(+) TCTGAG/AAGGCA 1 -- nc-transcript-variant1Minor allele frequency- A:0.03WA 118

HapMap Linkage Disequilibrium report for C11orf92 (111164114 - 111175770 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
      Database of Genomic Variants (DGV) variations for C11orf92: --

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

C11orf92 for disorders           About GeneDecksing

2 diseases for C11orf92:    About MalaCards
familial colorectal cancer    colorectal cancer

Human Genome Epidemiology (HuGE) Navigator: C11orf92 (0 documents)

Export disorders for C11orf92 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 C11orf92 gene integrated from 9 sources:
(articles sorted by number of sources associating them with C11orf92)
    Utopia: connect your pdf to the dynamic
world of online information

  1. Risk of genome-wide association study-identified gene tic variants for colorectal cancer in a Chinese population. (PubMed id 20530476)1 Xiong F....Lin D. (2010)
  2. Susceptibility genetic variants associated with color ectal cancer risk correlate with cancer phenotype. (PubMed id 20638935)1 AbulA- A....Andreu M. (2010)
  3. Association studies on 11 published colorectal cancer risk loci. (PubMed id 20648012)1 von Holst S....Lindblom A. (2010)
  4. Low-penetrance susceptibility variants in familial co lorectal cancer. (PubMed id 20501757)1 NiittymAoki I....Aaltonen L.A. (2010)
  5. Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort. (PubMed id 19843678)1 Middeldorp A....van Wezel T. (2009)
  6. Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer. (PubMed id 18753146)1 Pittman A.M....Houlston R.S. (2008)
  7. Human chromosome 11 DNA sequence and analysis including novel gene identification. (PubMed id 16554811)2 Taylor T.D....Sakaki Y. (2006)
  8. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)2 Ota T.... Sugano S. (2004)

(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: 399948 HGNC: 33789 AceView: FLJ45803 Ensembl:ENSG00000196167 euGenes: HUgn399948
ECgene: C11orf92 H-InvDB: C11orf92

(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 C11orf92 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 C11orf92 gene:
Search GeneIP for patents involving C11orf92

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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