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

CRYGN Gene

protein-coding   GIFtS: 44
GCID: GC07M151125

crystallin, gamma N

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

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

Aliases
Crystallin, Gamma N1 2
Gamma-N-Crystallin1
Gamma-Crystallin N2
GammaN-Crystallin1
Gamma-N-Crystallin1

External Ids:    HGNC: 204581   Entrez Gene: 1550512   Ensembl: ENSG000001273777   OMIM: 6096035   UniProtKB: Q8WXF53   

Export aliases for CRYGN gene to outside databases

Previous GC identifers: GC07M149373 GC07M150440 GC07M150517 GC07M150564 GC07M150757 GC07M144938


(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 CRYGN:
The beta and gamma crystallins are evolutionarily related families of proteins that are localized to the refractive
structure of the eye lens. The protein encoded by this gene is unique in that it has both beta and gamma crystallin
protein motifs. (provided by RefSeq, Jul 2008)




(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_000007.13  NC_018918.1  NT_007914.15  NT_079596.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the CRYGN gene promoter:
         STAT1   AML1a   AP-4   C/EBPalpha   FOXL1   CHOP-10   PPAR-gamma1   PPAR-gamma2   Zic3   TGIF   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmids (see all 2): CRYGN promoter sequence
   Search SABiosciences Chromatin IP Primers for CRYGN

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


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

Entrez Gene cytogenetic band: 7q36.1   Ensembl cytogenetic band:  7q36.1   HGNC cytogenetic band: 7q36.1

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

GeneLoc information about chromosome 7         GeneLoc Exon Structure

GeneLoc location for GC07M151125:  view genomic region     (about GC identifiers)

Start:
151,125,921 bp from pter      End:
151,137,899 bp from pter
Size:
11,979 bases      Orientation:
minus strand

1 alternative location:
Chr7-,CRA_TCAG 150,456,639-150,466,682     

(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: CRGN_HUMAN, Q8WXF5 (See protein sequence)
Recommended Name: Gamma-crystallin N  
Size: 182 amino acids; 20624 Da
Subunit: Monomer (By similarity)
Caution: In contrast to the orthologous protein found in other species, the C-terminal part differs and lacks the
fourth beta/gamma crystallin 'Greek key' domain. Moreover, its non-specific tissue specificity suggests that it may
have lost its function (PubMed:15853812)
Secondary accessions: Q496G6
Alternative splicing: 2 isoforms:  Q8WXF5-1   Q8WXF5-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for CRYGN: NX_Q8WXF5

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8WXF5

  • CRYGN Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_653328.1  
    ENSEMBL proteins: 
     ENSP00000338613   ENSP00000420157  

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

    CRYGN for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR001064 Beta/gamma_crystallin
     IPR011024 G_crystallin-rel

    Graphical View of Domain Structure for InterPro Entry Q8WXF5

    ProtoNet protein and cluster: Q8WXF5

    2 Blocks protein families:
    IPB001064 Beta and gamma crystallin
    IPB011024 Gamma-crystallin related


    UniProtKB/Swiss-Prot: CRGN_HUMAN, Q8WXF5
    Similarity: Belongs to the beta/gamma-crystallin family
    Similarity: Contains 3 beta/gamma crystallin 'Greek key' domains


    (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 CRYGN

    (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 CRYGN
    Search CenterWatch for drugs/clinical trials and news about CRYGN / CRGN 

    (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,
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    About This Section

    REFSEQ mRNAs for CRYGN gene: 
    NM_144727.1  

    Unigene Cluster for CRYGN:

    Crystallin, gamma N
    Hs.647104  [show with all ESTs]
    Unigene Representative Sequence: BM548090
    5 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000476631(uc003wkg.3) ENST00000462809 ENST00000337323(uc003wke.3)
    ENST00000491928(uc003wkf.3) ENST00000478106(uc010lqd.1)

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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat CRYGN
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    Additional cDNA sequence: 

    AF445455.1 BC100878.2 BC100879.3 BC100880.2 BC100881.2 EF491784.1 

    2 DOTS entries:

    DT.97793177  DT.97807740 

    7 AceView cDNA sequences:

    BU683519 AF445455 NM_144727 BM548090 CB993791 BC043605 BI003328 

    GeneLoc Exon Structure

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

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


    ECgene alternative splicing isoforms for CRYGN

    (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

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

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

    About this image

    CRYGN expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    1 LifeMap In Vivo Development Anatomical Compartment/Cell 
    Tissue Anatomical Compartment CellCategory (developmental path)
    EyeLensEye
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See CRYGN Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for CRYGN

    SOURCE GeneReport for Unigene cluster: Hs.647104

    UniProtKB/Swiss-Prot: CRGN_HUMAN, Q8WXF5
    Tissue specificity: Not specifically expressed in eye

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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for CRYGN

    (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 CRYGN gene from 3/11 species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves CRYGN1 crystallin, gamma N 70.74(n)
    61.87(a)
      428406  NM_001166674.2  NP_001160146.2 
    lizard
    (Anolis carolinensis)
    Reptilia CRYGN6
    --
    53(a)
    1 ↔ 1
    6(3937681-3950417)
    zebrafish
    (Danio rerio)
    Actinopterygii Dr.292032 Transcribed sequence with weak similarity to protein more 76.47(n)    CB359117.1 


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for CRYGN gene
    CRYBB32  CRYGB2  CRYBA42  CRYBA12  CRYBB22  CRYGD2  CRYGA2  CRYBB12  
    CRYGC2  CRYBA22  CRYGS2  
    9 SIMAP similar genes for CRYGN using alignment to 1 protein entry:     CRGN_HUMAN:
    CRYGS    CRYBB3    CRYBA2    CRYGA    CRYGB    CRYGC
    CRYBA1    CRYGD    CRYBA4

    CRYGN for paralogs           About GeneDecksing



    (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

    10/246 NCBI SNPs in CRYGN are shown (see all 246    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 7 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs624797891,2
    C,F,--151126556(+) TTTGCG/ACCAAA 1 -- ds50013Minor allele frequency- A:0.12NA 124
    rs1153344461,2
    F,--151126625(+) AGGAAC/TGAAAA 1 -- ds50011Minor allele frequency- T:0.07WA 118
    rs588952871,2
    C,--151126702(+) AACCTG/CTCTGT 1 -- ds50011Minor allele frequency- C:0.50WA 2
    rs1119684701,2
    --151126790(+) AGATTC/TCAGCT 1 -- ds50011Minor allele frequency- T:0.50CSA 2
    rs78083691,2
    C,F,A,H,--151126822(+) TCAGTG/ACTCCA 1 -- ds500118Minor allele frequency- A:0.15NS EA NA CSA WA 2340
    rs1915091871,2
    --151126838(+) ATTCAA/TCAACA 1 -- ds50010--------
    rs1170913081,2
    F,--151126840(+) TCATCA/GACATC 1 -- ds50011Minor allele frequency- G:0.03EA 120
    rs117689681,2
    C,F,A,H,--151126851(+) ATCACC/TATCAT 1 -- ds500119Minor allele frequency- T:0.07NS EA NA WA 2340
    rs1839898241,2
    --151126875(+) AGGTGA/CGAGAT 1 -- ds50010--------
    rs1133134481,2
    C,--151126943(+) TTGGAC/TGGCTG 1 -- ds50012Minor allele frequency- T:0.05CSA WA 120

    HapMap Linkage Disequilibrium report for CRYGN (151125921 - 151137899 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for CRYGN: --

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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

    CRYGN for disorders           About GeneDecksing

    OMIM gene information: 609603    OMIM disorders: --

    1 disease for CRYGN:    About MalaCards
    cataract


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

    1. Gamma-N-crystallin and the evolution of the betagamma-crystallin superfamily in vertebrates. (PubMed id 15853812)1, 2 Wistow G.... Vihtelic T. (2005)
    2. 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)
    3. Human chromosome 7: DNA sequence and biology. (PubMed id 12690205)1 Scherer S.W.... Tsui L.-C. (2003)
    4. 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)
    5. Genetics of crystallins: cataract and beyond. (PubMed id 19007775)9 Graw J. (2009)

    (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: 155051 HGNC: 20458 AceView: CRYGN Ensembl:ENSG00000127377 euGenes: HUgn155051
    ECgene: CRYGN H-InvDB: CRYGN

    (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 CRYGN 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 CRYGN gene:
    Search GeneIP for patents involving CRYGN

    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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    GeneCards Homepage - Last full update: 19 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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    VWF
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    von Willebrand factor
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