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

C8orf22 Gene

protein-coding   GIFtS: 36
GCID: GC08P049984

chromosome 8 open reading frame 22

 Explore 1 disease affiliated with
C8orf22 via our new
 Human Malady Compendium 
Biological research products
for C8orf22
    

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

Aliases
Chromosome 8 Open Reading Frame 221 2
Exocrine Differentiation And Proliferation Factor-Like Protein2 3
Pancreatic Progenitor Cell Differentiation And Proliferation Factor-Like
Protein2

External Ids:    HGNC: 317451   Entrez Gene: 4923072   Ensembl: ENSG000001683337   UniProtKB: Q8WWR93   

Export aliases for C8orf22 gene to outside databases

Previous GC identifers: GC00U916963 GC08P050148 GC08U900617 GC08P045448


(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_000008.10  NC_018919.1  NT_008183.19  
Regulatory elements:
   Search SABiosciences Regulatory transcription factor binding sites for C8orf22
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for C8orf22

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat C8orf22


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

Entrez Gene cytogenetic band: 8q11   Ensembl cytogenetic band:  8q11.21   HGNC cytogenetic band: 8q11.21

C8orf22 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
C8orf22 gene location

GeneLoc information about chromosome 8         GeneLoc Exon Structure

GeneLoc location for GC08P049984:  view genomic region     (about GC identifiers)

Start:
49,966,870 bp from pter      End:
49,988,649 bp from pter
Size:
21,780 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: PDPFL_HUMAN, Q8WWR9 (See protein sequence)
Recommended Name: Pancreatic progenitor cell differentiation and proliferation factor-like protein  
Size: 84 amino acids; 9188 Da
Secondary accessions: G3V137 Q8WVI1
Alternative splicing: 3 isoforms:  Q8WWR9-1   Q8WWR9-2   Q8WWR9-3   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for C8orf22: NX_Q8WWR9

C8orf22 Protein expression data from MOPED and PaxDb:    About this image 

Estimated protein expression log10 (pmol).

REFSEQ proteins (4 alternative transcripts): 
NP_001007177.1  NP_001243525.1  NP_001243526.1  NP_001243527.1  

ENSEMBL proteins: 
 ENSP00000430392   ENSP00000428773   ENSP00000382561   ENSP00000304926  

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

C8orf22 for domains           About GeneDecksing

1 InterPro domain/family:
 IPR026754 PPDPF

Graphical View of Domain Structure for InterPro Entry Q8WWR9

ProtoNet protein and cluster: Q8WWR9

UniProtKB/Swiss-Prot: PDPFL_HUMAN, Q8WWR9
Similarity: Belongs to the PPDPF family


(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 C8orf22

Gene Ontology (GO): 2 biological process terms (GO ID links to tree view):    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0007275multicellular organismal development IEA--
GO:0030154cell differentiation IEA--


C8orf22 for ontologies           About GeneDecksing



(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 C8orf22
Search CenterWatch for drugs/clinical trials and news about C8orf22 / PDPFL 

(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 C8orf22 gene (4 alternative transcripts): 
NM_001007176.4  NM_001256596.1  NM_001256597.1  NM_001256598.1  

Unigene Cluster for C8orf22:

Chromosome 8 open reading frame 22
Hs.49890  [show with all ESTs]
Unigene Representative Sequence: NM_001256598
4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
ENST00000517663 ENST00000522267 ENST00000399653(uc003xqq.4) ENST00000303202


miRNA
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Additional cDNA sequence: 

AJ276240.1 BC017981.1 

4 DOTS entries:

DT.97809210  DT.40113308  DT.40252905  DT.410749 

GeneLoc Exon Structure

3 Alternative Splicing Database (ASD) splice patterns (SP) for C8orf22    About this scheme

ExUns: 1a · 1b ^ 2 ^ 3 ^ 4 ^ 5a · 5b · 5c · 5d · 5e
SP1:                                -                           
SP2:                                -     -                     
SP3:                                                            


ECgene alternative splicing isoforms for C8orf22

(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

C8orf22 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: AACAGCTCCC

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

About this image
See C8orf22 Protein Expression from SPIRE MOPED and PaxDB
Genevestigator expression for C8orf22

SOURCE GeneReport for Unigene cluster: Hs.49890
    SABiosciences Custom PCR Arrays for C8orf22
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In Situ
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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 chordates.

Orthologs for C8orf22 gene from 1/5 species (see all 5)    About this table
Organism Taxonomic
classification
Gene Description Human
Similarity
Orthology
Type
Details
chicken
(Gallus gallus)
Aves C8orf226
Uncharacterized protein
58(a)
1 ↔ 1
2(111813588-111815627)
        Species with no ortholog for C8orf22

ENSEMBL Gene Tree for C8orf22 (if available)
TreeFam Gene Tree for C8orf22 (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

10/346 NCBI SNPs in C8orf22 are shown (see all 346    About this table
Genomic DataTranscription Related DataAllele Frequencies
SNP IDValidClinical
significance
Chr 8 posSequence#AA
Chg
TypeMore#Allele
freq
PopTotal
sample
More
----------
rs602882411,2
C,--49964923(+) CTTTT-/GCTGCA 1 -- us2k10--------
rs1394014921,2
--49964992(+) TTCCTA/TAATTT 1 -- us2k10--------
rs1140831031,2
F,--49965073(+) CCTCTT/AGGTAT 1 -- us2k11Minor allele frequency- A:0.03WA 118
rs1828686181,2
--49965117(+) TTTTTA/GGTTGA 1 -- us2k10--------
rs1433227531,2
--49965169(+) TAGGAG/TTAGAA 1 -- us2k10--------
rs69862061,2
C,F,H,--49965249(+) CATCAC/TGTGAT 1 -- us2k110Minor allele frequency- T:0.04NS EA NA CSA WA 681
rs1177269771,2
--49965304(+) CATAAT/CACATA 1 -- us2k11Minor allele frequency- C:0.01EA 120
rs1471299801,2
--49965346(+) TAAAAA/GTAATT 1 -- us2k10--------
rs1181372941,2
--49965471(+) AAAGCG/ACTAGA 1 -- us2k11Minor allele frequency- A:0.01NA 120
rs1403140521,2
--49965609(+) GACATG/TTATTC 1 -- us2k10--------

HapMap Linkage Disequilibrium report for C8orf22 (49966870 - 49988649 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
      Database of Genomic Variants (DGV) variations for C8orf22: --

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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

C8orf22 for disorders           About GeneDecksing

1 disease for C8orf22:    About MalaCards
pancreatitis


Export disorders for C8orf22 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 C8orf22 gene integrated from 9 sources:
(articles sorted by number of sources associating them with C8orf22)
    Utopia: connect your pdf to the dynamic
world of online information

  1. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
  2. Creation of genome-wide protein expression libraries using random activation of gene expression. (PubMed id 11329013)1, 2 Harrington J.J.... Ducar M. (2001)
  3. 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)
  4. DNA sequence and analysis of human chromosome 8. (PubMed id 16421571)2 Nusbaum C....Lander E.S. (2006)
  5. 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)
  6. Hepatitis C virus core protein interacts with 14-3-3 protein and activates the kinase Raf-1. (PubMed id )2 Aoki H.... Hino O. (2000)

(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: 492307 HGNC: 31745 Ensembl:ENSG00000168333 euGenes: HUgn492307 ECgene: C8orf22
H-InvDB: C8orf22

(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 C8orf22 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 C8orf22 gene:
Search GeneIP for patents involving C8orf22

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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