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

MIR22HG Gene

RNA gene   GIFtS: 31
GCID: GC17M001616

MIR22 host gene (non-protein coding)

(Previous name: chromosome 17 open reading frame 91 )
(Previous symbol: C17orf91)
  Search for MIR22HG
in our new
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(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Subcategory (RNA class): lncRNA

Quality score for this RNA gene is 3

Aliases
MIR22 Host Gene (Non-Protein Coding)1 2
C17orf911 2 3
DKFZp686O061591
MGC143761
Chromosome 17 Open Reading Frame 911

External Ids:    HGNC: 282191   Entrez Gene: 849812   Ensembl: ENSG000001865947   UniProtKB: Q0VDD53   
ORGUL members:         
NONCODE:n408292 n408293 n408295 n377677    

Export aliases for MIR22HG gene to outside databases


(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_000017.10  NC_018928.1  NT_010718.16  
Regulatory elements:
   Search SABiosciences Regulatory transcription factor binding sites for MIR22HG
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for MIR22HG

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat MIR22HG


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

Entrez Gene cytogenetic band: 17p13.3   Ensembl cytogenetic band:  17p13.3   HGNC cytogenetic band: 17p13.3

MIR22HG Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
MIR22HG gene location

GeneLoc information about chromosome 17         GeneLoc Exon Structure

GeneLoc location for GC17M001616:  view genomic region     (about GC identifiers)

Start:
1,614,798 bp from pter      End:
1,620,468 bp from pter
Size:
5,671 bases      Orientation:
minus strand
ORGUL member locations:
Legend (see complete legend)

  • n408295
  • n408293
  • n408292
  • n377677
1614797 1617182 1619566 chr17

(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: CQ091_HUMAN, Q0VDD5 (See protein sequence)
Recommended Name: Putative uncharacterized protein encoded by MIR22HG  
Size: 57 amino acids; 6478 Da
Caution: Product of a dubious CDS prediction. May be a non-coding RNA
Secondary accessions: Q0VDD6

Explore the universe of human proteins at neXtProt for MIR22HG: NX_Q0VDD5

MIR22HG Protein expression data from MOPED and PaxDb: --

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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: Q0VDD5


(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 MIR22HG

(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 MIR22HG
Search CenterWatch for drugs/clinical trials and news about MIR22HG 

(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 MIR22HG gene (2 alternative transcripts): 
NM_001001870.1  NM_032895.2  

Unigene Cluster for MIR22HG:

MIR22 host gene (non-protein coding)
Hs.597755  [show with all ESTs]
Unigene Representative Sequence: BX648321
12 Ensembl transcripts including schematic representations, and UCSC links where relevant:
ENST00000334146(lincRNA)(uc002ftf.3) ENST00000574306(lincRNA)(uc002ftg.3 uc021tni.1 uc021tnj.1)
ENST00000576749(lincRNA) ENST00000570416(lincRNA) ENST00000571595(lincRNA) ENST00000571091(lincRNA) ENST00000573127(lincRNA)
ENST00000576489(lincRNA) ENST00000575626(lincRNA) ENST00000573075(lincRNA) ENST00000574016(lincRNA) ENST00000577164(lincRNA)


miRNA
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Inhib. RNA
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Additional cDNA sequence: 

AF070569.1 BC007813.2 BC070225.1 BC119720.1 BC119721.1 BX640650.1 BX648321.1 NR_028502.1 
NR_028503.1 NR_028504.1 NR_028505.1 

7 DOTS entries:

DT.455644  DT.100776839  DT.100017602  DT.91826492  DT.120948548  DT.120948593  DT.97842858 

24/156 AceView cDNA sequences (see all 156):

AA434535 CA309565 AI952239 NM_032895 BG482710 BM126997 AI344594 BE710277 
CR615473 AA257091 AL545472 CA309715 BQ030155 BE710283 BG289254 AA565303 
CA305977 AA443422 AW103633 AW804377 CR591309 BQ129198 BQ029784 BQ183272 

GeneLoc Exon Structure

3 Alternative Splicing Database (ASD) splice patterns (SP) for MIR22HG    About this scheme

ExUns: 1a · 1b · 1c ^ 2 ^ 3a · 3b · 3c ^ 4
SP1:                                -     -         
SP2:                                                
SP3:                    -                           


ECgene alternative splicing isoforms for MIR22HG

(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 MIR22HG:none

MIR22HG expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: TTATGTGATT

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

About this image
Genevestigator expression for MIR22HG

SOURCE GeneReport for Unigene cluster: Hs.597755
    SABiosciences Custom PCR Arrays for MIR22HG
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 MIR22HG gene from 1 species (see representative species )    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
mouse
(Mus musculus)
Mammalia Mir22hg5 RIKEN cDNA 2210403K04 gene   --   11 (45.91 cM) 75461539 


ENSEMBL Gene Tree for MIR22HG (if available)
TreeFam Gene Tree for MIR22HG (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

10/122 NCBI SNPs in MIR22HG are shown (see all 122    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 17 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs1858906371,2
--1614300(+) CGGAGA/GAGCCT 5 -- int1 us2k10--------
rs1911376231,2
--1614342(+) GGCCCC/TCAGTC 5 -- int1 us2k10--------
rs1475854381,2
--1614392(+) GGGTGA/GGTAGA 5 -- int1 us2k10--------
rs777054051,2
F,--1614547(+) TCCCCC/TAGCCC 5 -- int1 us2k11Minor allele frequency- T:0.10WA 118
rs757166771,2
C,--1614709(+) CAAGAG/CGTGCC 5 -- us2k1 int12Minor allele frequency- C:0.04NA 122
rs1829893521,2
--1614768(+) TACCCC/TCACCT 5 -- int1 us2k10--------
rs106540091,2
C,F,--1614812(+) AATTATATT/-  
        
TATTA
5 -- us2k1 nc-transcript-variant2Minor allele frequency- -:0.50NA CSA 4
rs760420621,2
--1614812(+) AAATTA/TTATTA 5 -- nc-transcript-variantus2k10--------
rs58188261,2
C--1614816(+) ATATTTATT/-  
        
ATATG
5 -- us2k1 nc-transcript-variant1Minor allele frequency- -:0.00NA 2
rs1421107231,2
--1614912(+) CACTCA/GACATT 5 -- us2k1 nc-transcript-variant0--------

HapMap Linkage Disequilibrium report for MIR22HG (1614798 - 1620468 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
      Database of Genomic Variants (DGV) variations for MIR22HG: --

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
  --

(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 MIR22HG gene integrated from 9 sources:
(articles sorted by number of sources associating them with MIR22HG)
    Utopia: connect your pdf to the dynamic
world of online information

  1. Large-scale concatenation cDNA sequencing. (PubMed id 9110174)1, 3 Yu W.... Gibbs R.A. (1997)
  2. A "double adaptor" method for improved shotgun library construction. (PubMed id 8619474)1, 3 Andersson B.... Gibbs R.A. (1996)
  3. Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. (PubMed id 20705733)1 O'Seaghdha C.M....KAPttgen A. (2010)
  4. 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)
  5. Transcriptome analysis of human gastric cancer. (PubMed id 16341674)1 Oh J.H....Kim N.S. (2005)
  6. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)2 Gerhard D.S....Malek J. (2004)
  7. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (PubMed id 12477932)1 Strausberg R.L....Marra M.A. (2002)

(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: 84981 HGNC: 28219 AceView: MGC14376 Ensembl:ENSG00000186594 euGenes: HUgn84981
ECgene: MIR22HG H-InvDB: MIR22HG

(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 MIR22HG 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 MIR22HG gene:
Search GeneIP for patents involving MIR22HG

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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