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

SNX21 Gene

protein-coding   GIFtS: 46
GCID: GC20P044462

Sorting Nexin Family Member 21

(Previous name: chromosome 20 open reading frame 161)
(Previous symbol: C20orf161)
  Search for SNX21
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
Sorting Nexin Family Member 211 2     PP39932
C20orf1611 2 3     dJ337O18.42
Sorting Nexin L2 3     Sorting Nexin 212
SNX-L2 3     Sorting Nexin-212
Chromosome 20 Open Reading Frame 1611     SNXL3

External Ids:    HGNC: 161541   Entrez Gene: 902032   Ensembl: ENSG000001241047   UniProtKB: Q969T33   

Export aliases for SNX21 gene to outside databases

Previous GC identifers: GC20P043896 GC20P041204


(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 SNX21 Gene:
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which
is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not
contain a coiled coil region, like some family members. The specific function of this protein has not been
determined. Multiple transcript variants encoding distinct isoforms have been identified for this gene. (provided
by RefSeq, Jul 2008)

GeneCards Summary for SNX21 Gene: 
SNX21 (sorting nexin family member 21) is a protein-coding gene. GO annotations related to this gene include phosphatidylinositol binding. An important paralog of this gene is SNX20.

UniProtKB/Swiss-Prot: SNX21_HUMAN, Q969T3
Function: May be involved in several stages of intracellular trafficking (By similarity)

Gene Wiki entry for SNX21 Gene


(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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000020.10  NT_011362.10  NC_018931.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SNX21 gene promoter:
         Egr-3   Max1   AhR   MyoD   Lmo2   Arnt   Egr-2   HFH-1   Msx-1   c-Myc   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSNX21 promoter sequence
   Search SABiosciences Chromatin IP Primers for SNX21

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SNX21


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

Entrez Gene cytogenetic band: 20q13.12   Ensembl cytogenetic band:  20q13.12   HGNC cytogenetic band: 20q13.12

SNX21 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SNX21 gene location

GeneLoc information about chromosome 20         GeneLoc Exon Structure

GeneLoc location for GC20P044462:  view genomic region     (about GC identifiers)

Start:
44,462,449 bp from pter      End:
44,471,914 bp from pter
Size:
9,466 bases      Orientation:
plus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: SNX21_HUMAN, Q969T3 (See protein sequence)
Recommended Name: Sorting nexin-21  
Size: 373 amino acids; 41365 Da
Subcellular location: Cytoplasmic vesicle membrane; Peripheral membrane protein; Cytoplasmic side (By similarity)
Secondary accessions: Q5JZH5 Q5JZH6 Q5JZH7 Q8WUR6 Q9BR16
Alternative splicing: 3 isoforms:  Q969T3-1   Q969T3-2   Q969T3-3   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for SNX21: NX_Q969T3

Explore proteomics data for SNX21 at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q969T3

  • SNX21 Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    SNX21 Protein Expression
    REFSEQ proteins (4 alternative transcripts): 
    NP_001036097.1  NP_001036098.1  NP_219489.1  NP_690857.1  

    ENSEMBL proteins: 
     ENSP00000420169   ENSP00000418593   ENSP00000344586   ENSP00000361620   ENSP00000361619  

    Human Recombinant Protein Products for SNX21: 
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    Novus Biologicals SNX21 Protein
    Novus Biologicals SNX21 Lysates
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Cloud-Clone Corp. Proteins for SNX21 

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0030659cytoplasmic vesicle membrane IEA--

    SNX21 for ontologies           About GeneDecksing



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    Cloud-Clone Corp. ELISAs for SNX21 
    Cloud-Clone Corp. CLIAs for SNX21


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    HGNC Gene Families: 
    TTC: Tetratricopeptide (TTC) repeat domain containing
    SNX: Sorting nexins

    2 InterPro protein domains:
     IPR011990 TPR-like_helical
     IPR001683 Phox

    Graphical View of Domain Structure for InterPro Entry Q969T3

    ProtoNet protein and cluster: Q969T3

    1 Blocks protein domain: IPB001683 Phox-like

    UniProtKB/Swiss-Prot: SNX21_HUMAN, Q969T3
    Domain: The PX domain mediates specific binding to membranes enriched in phosphatidylinositol 3-phosphate
    (PtdIns(P3)) (By similarity)
    Similarity: Belongs to the sorting nexin family
    Similarity: Contains 1 PX (phox homology) domain


    SNX21 for domains           About GeneDecksing


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

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: SNX21_HUMAN, Q969T3
    Function: May be involved in several stages of intracellular trafficking (By similarity)

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding ----
    GO:0035091phosphatidylinositol binding IEA--
         
    SNX21 for ontologies           About GeneDecksing


    Phenotypes:
         2 GenomeRNAi human phenotypes for SNX21:
     Decreased melanin production  Increased G1 DNA content 

    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for SNX21 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for SNX21

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for SNX21 
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for SNX21 

    miRNA
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    hsa-miR-607 hsa-miR-520e hsa-miR-302d hsa-miR-520f hsa-miR-146a hsa-miR-106a hsa-miR-10b* hsa-miR-1304
    SwitchGear 3'UTR luciferase reporter plasmidSNX21 3' UTR sequence
    Inhib. RNA
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, 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 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for SNX21

    STRING Interaction Network Preview (showing 1 interactants - click image to see more details)

    1 Interacting protein for SNX21 (ENSP000004185934) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    COX6A2ENSP000002874904STRING: ENSP00000287490
    About this table

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0007154cell communication IEA--
    GO:0015031protein transport IEA--

    SNX21 for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, 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 SNX21

    Search CenterWatch for drugs/clinical trials and news about SNX21

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for SNX21 gene (4 alternative transcripts): 
    NM_001042632.1  NM_001042633.1  NM_033421.2  NM_152897.1  

    Unigene Cluster for SNX21:

    Sorting nexin family member 21
    Hs.472854  [show with all ESTs]
    Unigene Representative Sequence: NM_001042633
    12 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000466252 ENST00000462307 ENST00000472219 ENST00000491381 ENST00000342644
    ENST00000372542 ENST00000372541 ENST00000344780(uc002xpt.1 uc002xps.1 uc002xpu.1 uc002xpv.1 uc002xpw.1 uc010zxd.1)
    ENST00000478230 ENST00000372547(uc002xpy.1) ENST00000486336 ENST00000465997

    miRNA
    Products:
         
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    8/34 QIAGEN miScript miRNA Assays for microRNAs that regulate SNX21 (see all 34):
    hsa-miR-607 hsa-miR-520e hsa-miR-302d hsa-miR-520f hsa-miR-146a hsa-miR-106a hsa-miR-10b* hsa-miR-1304
    SwitchGear 3'UTR luciferase reporter plasmidSNX21 3' UTR sequence
    Inhib. RNA
    Products:
         
    Browse for Gene Knock-down Tools from EMD Millipore
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    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat SNX21
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    GenScript: all cDNA clones in your preferred vector (see all 4): SNX21 (NM_152897)
    DNA2.0 Custom Codon Optimized Gene Synthesis Service for SNX21
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat SNX21
    Sirion Biotech Customized lentivirus for stable overexpression of SNX21 
                         Customized lentivirus expression plasmids for stable overexpression of SNX21 
    Primer
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      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat SNX21

    Additional mRNA sequence: 

    AF395845.1 AF523834.1 AK091359.1 AK095851.1 AK226120.1 AK293443.1 AK297622.1 AL591562.1 
    BC012904.1 BC019823.1 

    11 DOTS entries:

    DT.97852110  DT.97775420  DT.40213032  DT.100707832  DT.120817362  DT.439019  DT.100812146  DT.95336060 
    DT.100028476  DT.100812149  DT.95336063 

    24/121 AceView cDNA sequences (see all 121):

    AA365779 BU687546 AW450013 BM677889 CD369894 AF523834 NM_033421 AI915413 
    Z39581 AA365778 AL591562 CR617424 AF395845 CR601928 BQ771786 AI935964 
    NM_152897 BM142124 AW173296 CK819910 BF061958 AI376594 BC019823 BM722860 

    GeneLoc Exon Structure

    5/8 Alternative Splicing Database (ASD) splice patterns (SP) for SNX21 (see all 8)    About this scheme

    ExUns: 1a · 1b · 1c ^ 2 ^ 3 ^ 4a · 4b · 4c ^ 5 ^ 6 ^ 7a · 7b · 7c
    SP1:                                -           -                                 
    SP2:                                -           -     -                           
    SP3:                                -                                             
    SP4:                                -                 -                           
    SP5:                                                                              


    ECgene alternative splicing isoforms for SNX21

    (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

    SNX21 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: TCCGGCTCTC
    SNX21 Expression
    About this image


    See SNX21 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SNX21

    SOURCE GeneReport for Unigene cluster: Hs.472854

    UniProtKB/Swiss-Prot: SNX21_HUMAN, Q969T3
    Tissue specificity: Highly expressed in fetus liver, but only weakly expressed in brain, skeleton muscle, smooth
    muscle, and cardiac muscle, kidney, and adrenal gland

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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 animals.

    Orthologs for SNX21 gene from 5/11 species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Snx211 , 5 sorting nexin family member 211, 5 88.15(n)1
    93.94(a)1
      2 (85.27 cM)5
    1011131  NM_133924.31  NP_598685.21 
     1647858235 
    chicken
    (Gallus gallus)
    Aves SNX211 sorting nexin family member 21 68.52(n)
    61.28(a)
      419302  XM_417474.3  XP_417474.3 
    lizard
    (Anolis carolinensis)
    Reptilia SNX216
    Uncharacterized protein
    50(a)
    1 ↔ 1
    AAWZ02036440(3231-3596)
    zebrafish
    (Danio rerio)
    Actinopterygii snx211 sorting nexin family member 21 53.19(n)
    47.65(a)
      555580  NM_001077368.2  NP_001070836.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG30771 CG3077 43.14(n)
    30.1(a)
      33466  NM_134865.2  NP_608709.1 


    ENSEMBL Gene Tree for SNX21 (if available)
    TreeFam Gene Tree for SNX21 (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SNX21 gene
    SNX202  
    2 SIMAP similar genes for SNX21 using alignment to 4 protein entries:     SNX21_HUMAN (see all proteins):
    C20orf161    SNX20

    SNX21 for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, 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

    10/251 SNPs in SNX21 are shown (see all 251)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 20 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1177282111,2
    C,F--44460740(+) GAGGCC/TAGGTG 4 -- us2k11Minor allele frequency- T:0.01NA 120
    rs736226101,2
    C,F--44460781(+) CCCCAC/TCTCTA 4 -- us2k10--------
    rs61309411,2
    C,F,H--44460813(+) GCATGG/TTGGCA 4 -- us2k19Minor allele frequency- T:0.18NS EA NA 664
    rs1382077491,2
    C--44460862(+) GAGAAC/TTGCTT 4 -- us2k10--------
    rs1903501591,2
    --44460902(+) CAAGAC/TTGCAT 4 -- us2k10--------
    rs2012346971,2
    --44460957(+) TCTAA-/AAAT  
            
    AAATA
    4 -- us2k10--------
    rs1422315201,2
    C--44461070(+) ATCTTC/GAAAAT 4 -- us2k10--------
    rs73453161,2
    C--44461081(+) ggaccA/Cttaat 4 -- us2k12Minor allele frequency- C:0.00NA 4
    rs1431814721,2
    --44461126(+) GGGAGA/GGATGT 4 -- us2k10--------
    rs1818950441,2
    --44461178(+) CAGAAA/TATAAG 4 -- us2k10--------

    HapMap Linkage Disequilibrium report for SNX21 (44462449 - 44471914 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for SNX21:    About this table     
    Variant IDTypeSubtypePubMed ID
    nsv458993CNV Loss19166990
    nsv833990CNV Loss17160897

    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing SNX21
    DNA2.0 Custom Variant and Variant Library Synthesis for SNX21

    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, 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 SNX21 gene, integrated from 9 sources (see all 12):
    (articles sorted by number of sources associating them with SNX21)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Expression of a novel member of sorting nexin gene family, SNX-L, in human liver development. (PubMed id 12459172)1, 2, 3, 9 Zeng W.... Liu M. (2002)
    2. Sorting out the cellular functions of sorting nexins. (PubMed id 12461558)1, 3 Worby C.A. and Dixon J.E. (2002)
    3. The DNA sequence and comparative analysis of human chromosome 20. (PubMed id 11780052)1, 2 Deloukas P....Rogers J. (2001)
    4. Toward an understanding of the protein interaction net work of the human liver. (PubMed id 21988832)1 Wang J....Yang X. (2011)
    5. Interactions of pathological hallmark proteins: tubul in polymerization promoting protein/p25, beta-amyloid, and alpha-synuclein. (PubMed id 21832049)1 OlA!h J....OvA!di J. (2011)
    6. 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)
    7. 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)
    8. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1 Ota T.... Sugano S. (2004)
    9. 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)
    10. A large family of endosome-localized proteins related to sorting nexin 1. (PubMed id 11485546)1 Teasdale R.D.... Gleeson P.A. (2001)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 90203 HGNC: 16154 AceView: C20orf161 Ensembl:ENSG00000124104 euGenes: HUgn90203
    ECgene: SNX21 H-InvDB: SNX21

    (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 SNX21 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 SNX21 gene:
    Search GeneIP for patents involving SNX21

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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