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

HCG9 Gene

RNA gene   GIFtS: 37
GCID: GC06P029943

HLA complex group 9 (non-protein coding)

(Previous name: HLA complex group 9 )
 Explore 5 diseases affiliated with
HCG9 via our new
 Human Malady Compendium 
Biological research products
for HCG9
    

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

Subcategory (RNA class): processed_transcript

Quality score for this RNA gene is 3

Aliases
HLA Complex Group 9 (Non-Protein Coding)1 2     PERB111
HCGIX1 2 4     HCG IX4
HCGIX41 2     HcgIX1
HLA Complex Group 91 4     HcgIX Protein4
HCGIX-41     

External Ids:    HGNC: 212431   Entrez Gene: 102552   Ensembl: ENSG000002046257   UniProtKB: Q930654   

Export aliases for HCG9 gene to outside databases

Previous GC identifers: GC06P029713 GC06P030048 GC06P030050


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

Entrez Gene summary for HCG9:
This gene lies within the MHC class I region on chromosome 6p21.3. This gene is believed to be non-coding, but its
function has not been determined. (provided by RefSeq, Jul 2009)




(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_000006.11  NC_018917.1  NT_007592.15  NT_113891.2  NT_167245.1  NT_167246.1  NT_167247.1  NT_167248.1  
NT_167249.1  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the HCG9 gene promoter:
         AML1a   p300   SREBP-1c   HTF   SREBP-1b   AREB6   SREBP-1a   ARP-1   ATF   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidHCG9 promoter sequence
   Search SABiosciences Chromatin IP Primers for HCG9

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat HCG9


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

Entrez Gene cytogenetic band: 6p21.3   Ensembl cytogenetic band:  6p22.1   HGNC cytogenetic band: 6p21.3

HCG9 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
HCG9 gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06P029943:  view genomic region     (about GC identifiers)

Start:
29,942,889 bp from pter      End:
29,946,183 bp from pter
Size:
3,295 bases      Orientation:
plus strand

6 alternative locations:
Chr6+,ALT_REF_LOCI_3 29,932,826-29,947,156      Chr6+,ALT_REF_LOCI_6 29,932,284-29,971,159      Chr6+,ALT_REF_LOCI_4 29,861,132-29,864,418     
Chr6+,ALT_REF_LOCI_5 29,936,176-29,939,465      Chr6+,ALT_REF_LOCI_2 29,932,391-29,974,868      Chr6+,ALT_REF_LOCI_7 29,861,681-29,864,967     

(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/TrEMBL: Q93065 (See protein sequence)
Recommended Name: HCG IX  
Size: 77 amino acids; 8694 Da


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

ProtoNet protein and cluster: Q93065


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

Phenotypes:
     1 GenomeRNAi human phenotype for HCG9:
 Synthetic lethal with Ras 

Animal Models:
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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 HCG9

(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 HCG9
Search CenterWatch for drugs/clinical trials and news about HCG9 

(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 HCG9 gene: 
NM_005844.2  

Unigene Cluster for HCG9:

HLA complex group 9 (non-protein coding)
Hs.656251  [show with all ESTs]
Unigene Representative Sequence: BX097961
2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
ENST00000376800(lincRNA)(uc003rth.3) ENST00000463275(lincRNA)

miRNA
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Additional cDNA sequence: 

AK289926.1 BC119792.1 NR_028032.1 X95289.1 

2 DOTS entries:

DT.307579  DT.91802280 

2 AceView cDNA sequences:

NM_005844 X95289 

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

Expression evidence for HCG9:none

HCG9 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: AGCTTCTACC
HCG9 Expression
About this image
Genevestigator expression for HCG9

SOURCE GeneReport for Unigene cluster: Hs.656251
    SABiosciences Custom PCR Arrays for HCG9

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
  --

ENSEMBL Gene Tree for HCG9 (if available)
TreeFam Gene Tree for HCG9 (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

10/50 NCBI SNPs in HCG9 are shown (see all 50    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 6 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs1156724791,2
--29945533(+) ACAAAA/CTCAAA 1 -- int10--------
rs92608611,2
C,F,H--29945594(+) TTGCAC/TACAAT 1 -- int19Minor allele frequency- T:0.03NS EA CSA WA NA 774
rs22461981,2
C,F,H--29945602(+) AATCAG/ATGTAT 1 -- int115Minor allele frequency- A:0.21NS EA WA CSA NA 1202
rs22461991,2
C,F,H--29945620(+) AAATGC/TACAGC 1 -- int117Minor allele frequency- T:0.19NS EA WA NA 2326
rs1908671531,2
--29945677(+) TACCAC/TAATGA 1 -- int10--------
rs92608621,2
C,F,H--29945741(+) TTCCAC/TGCAGT 1 -- int110Minor allele frequency- T:0.06NS EA NA CSA WA 784
rs92608631,2
C,F,H--29945771(+) AATTTG/TTAAGT 1 -- int19Minor allele frequency- T:0.06NS EA CSA WA NA 758
rs560526121,2
C--29945802(+) GCCCAG/CCCTAC 1 -- int14Minor allele frequency- C:0.22WA EA 242
rs1152481111,2
--29945830(+) AGGACA/GAGGAT 1 -- int10--------
rs92608641,2
C,F,H--29945841(+) ATATGG/AAATTA 1 -- int19Minor allele frequency- A:0.06NS EA NA CSA WA 760

HapMap Linkage Disequilibrium report for HCG9 (29942889 - 29946183 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
Database of Genomic Variants (DGV): 6 variations for HCG9
     6 CNVs: 99484 7558 4669 31269 3599 2622

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

HCG9 for disorders           About GeneDecksing

5 diseases for HCG9:    About MalaCards
systemic lupus erythematosus    lupus erythematosus    multiple sclerosis    hodgkin's lymphoma
vitiligo

Human Genome Epidemiology (HuGE) Navigator: HCG9 (4 documents)

Export disorders for HCG9 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 HCG9 gene, integrated from 9 sources (see all 12):
(articles sorted by number of sources associating them with HCG9)
    Utopia: connect your pdf to the dynamic
world of online information

  1. Molecular dynamics of MHC genesis unraveled by sequence analysis of the 1,796,938-bp HLA class I region. (PubMed id 10557312)1, 3 Shiina T....Inoko H. (1999)
  2. A 356-Kb sequence of the subtelomeric part of the MHC class I region. (PubMed id 10727083)1, 3 Hampe A.... Galibert F. (1999)
  3. A genome-wide association study in Han Chinese identif ies multiple susceptibility loci for IgA nephropathy. (PubMed id 22197929)1 Yu X.Q....Liu J.J. (2012)
  4. A multi-tissue analysis identifies HLA complex group 9 gene methylation differences in bipolar disorder. (PubMed id 21647149)1 Kaminsky Z....Petronis A. (2012)
  5. Variant of TYR and autoimmunity susceptibility loci i n generalized vitiligo. (PubMed id 20410501)1 Jin Y....Spritz R.A. (2010)
  6. A major histocompatibility Class I locus contributes to multiple sclerosis susceptibility independently from HLA-DRB1*15:01. (PubMed id 20593013)1 Cree B.A.... . (2010)
  7. High-density SNP screening of the major histocompatib ility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions. (PubMed id 19851445)1 Barcellos L.F....Criswell L.A. (2009)
  8. Rapid evolution of major histocompatibility complex class I genes in primates generates new disease alleles in humans via hitchhiking diversity. (PubMed id 16702430)1 Shiina T.... Bahram S. (2006)
  9. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. (PubMed id 16344560)1 Kimura K.... Sugano S. (2006)
  10. Physical map of the HLA-A/HLA-F subregion and identification of two new coding sequences. (PubMed id 8575815)1 Pichon L....David V. (1996)

(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: 10255 HGNC: 21243 AceView: HCG9 Ensembl:ENSG00000204625 euGenes: HUgn10255
ECgene: HCG9 H-InvDB: HCG9

(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 HCG9 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 HCG9 gene:
Search GeneIP for patents involving HCG9

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 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript, LifeMap BioReagents, and Sirion Biotech, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences, In Situ Hybridization Assays from
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