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SNX21 Gene

protein-coding   GIFtS: 46
GCID: GC20P044462

Sorting Nexin Family Member 21

(Previous name: chromosome 20 open reading frame 161)
(Previous symbol: C20orf161)
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(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
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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, GeneCards, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
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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 75), Regulatory elements and Epigenetics data according to QIAGEN, and/or SwitchGear Genomics)
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RefSeq DNA sequence at NCBI GenBank:
NC_000020.10  NT_011362.11  NC_018931.2  
Regulatory elements:
   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 Chromatin IP Primers for SNX21

Epigenetics:
DNA Methylation CpG Assay Predesigned for Pyrosequencing 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 1UniProtKB, HORDE, 2neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, 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, Cloud-Clone Corp., and/or eBioscience,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, Cloud-Clone Corp., and/or eBioscience, Antibodies by EMD Millipore, R&D Systems, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, Cloud-Clone Corp, and/or others.)
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UniProtKB/Swiss-Prot: SNX21_HUMAN, Q969T3 (See protein sequence)
Recommended Name: Sorting nexin-21  
Size: 373 amino acids; 41365 Da
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


See SNX21 Protein Expression from SPIRE MOPED, PaxDB, and MaxQB

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

ENSEMBL proteins: 
 ENSP00000420169   ENSP00000418593   ENSP00000344586   ENSP00000361620   ENSP00000361619  

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Search eBioscience for ELISAs for SNX21 


(According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
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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


Find genes that share domains with SNX21           About GenesLikeMe


(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,
transcription factor targeting from QIAGEN and/or HOMER, miRNA Gene Targets from miRTarBase, shRNA from OriGene, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, SwitchGear Genomics, Gene Editing from DNA2.0, Clones from OriGene, GenScript, Sino Biological, DNA2.0, Vector BioLabs and/or Addgene, Cell Lines from GenScript, ESI BIO, In Situ Hybridization Assays from Advanced Cell Diagnostics, Flow cytometry from eBioscience, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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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:    About this table

GO IDQualified GO termEvidencePubMed IDs
GO:0005515protein binding ----
GO:0035091phosphatidylinositol binding IEA--
     
Find genes that share ontologies with SNX21           About GenesLikeMe


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

Animal Models:
   inGenious Targeting Laboratory: Let us create your new Knockout/Knockin mouse model for SNX21
   inGenious Targeting Laboratory: Contact us about creating complex and humanized mouse models 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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Block miRNA regulation of human, mouse, rat SNX21 using miScript Target Protectors
Selected qRT-PCR 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
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Predesigned siRNA for gene silencing in human, mouse, rat SNX21

Gene Editing
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GenScript: all cDNA clones in your preferred vector (see all 4): SNX21 (NM_152897)
Browse Sino Biological Human cDNA Clones
DNA2.0 Custom Codon Optimized Gene Synthesis Service for SNX21
Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat SNX21

Cell Line
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In Situ Assay
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Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SNX21


(According to UniProtKB, COMPARTMENTS Subcellular localization database, Ontologies according to Gene Ontology Consortium 01 Apr 2014 via Entrez Gene.)
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Subcellular locations from UniProtKB/Swiss-Prot
SNX21_HUMAN, Q969T3: Cytoplasmic vesicle membrane; Peripheral membrane protein; Cytoplasmic side (By similarity)
Subcellular locations from COMPARTMENTS: 

CompartmentConfidence
cytosol3
nucleus2
mitochondrion1

Gene Ontology (GO): 1 cellular component term:    About this table

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

Find genes that share ontologies with SNX21           About GenesLikeMe


(SuperPaths according to PathCards, Pathways according to 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 QIAGEN, 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 Apr 2014 via Entrez Gene).
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    Custom Pathway & Disease-focused RT2 Profiler PCR Arrays for SNX21
Interactions:

    Search GeneGlobe Interaction Network for SNX21

STRING Interaction Network Preview (showing 2 interactants - click image to see more details)

2 Interacting proteins for SNX21 (ENSP000004185934) via UniProtKB, MINT, STRING, and/or I2D
InteractantInteraction Details
GeneCardExternal ID(s)
C19orf12ENSP000003761034STRING: ENSP00000376103
COX6A2ENSP000002874904STRING: ENSP00000287490
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Gene Ontology (GO): 2 biological process terms:    About this table

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

Find genes that share ontologies with SNX21           About GenesLikeMe



(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience, ApexBio, HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB)
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Browse Small Molecules at EMD Millipore
   Browse drugs & compounds from Enzo Life Sciences
  Browse compounds at ApexBio 

Browse Tocris compounds for 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,
exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN, SwitchGear Genomics,
Tagged/untagged cDNA clones from OriGene, GenScript, DNA2.0, Vector BioLabs, and/or Addgene, Primers from OriGene, and/or QIAGEN, Flow cytometry from eBioscience )
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REFSEQ mRNAs for SNX21 gene (4 alternative transcripts): 
NM_001042632.2  NM_001042633.2  NM_033421.3  NM_152897.2  

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:
     
Block miRNA regulation of human, mouse, rat SNX21 using miScript Target Protectors
Selected qRT-PCR 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:
     
OriGene RNAi products in human, mouse, rat for SNX21
Predesigned siRNA for gene silencing in human, mouse, rat SNX21
Clone
Products:
     
OriGene clones in human, mouse for SNX21 (see all 21)
OriGene ORF clones in mouse, rat for SNX21
OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
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
Primer
Products:
    
OriGene qPCR primer pairs and template standards for SNX21
OriGene qSTAR qPCR primer pairs in human, mouse for SNX21
Pre-validated RT2 qPCR Primer Assay in human, mouse, rat SNX21
  QuantiTect SYBR Green Assays in human, mouse, rat SNX21
  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 

Selected AceView cDNA sequences (see all 121):

AA365778 AW173296 AA365779 NM_033421 AW450013 CR601928 BU687546 NM_152897 
BM142124 AI935964 CK819910 BQ771786 AI376594 BM677889 AL591562 CD369894 
CR617424 AF523834 AI915413 AF395845 BF061958 Z39581 BM822554 Z43509 

GeneLoc Exon Structure

Selected 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™, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MaxQB, plus additional links to SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from QIAGEN, Primers from OriGene, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
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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

SNX21 Protein expression data from MOPED1, PaxDb2 and MaxQB3    About this image

SNX21 Protein Expression

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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QuantiFast Probe-based Assays in human, mouse, rat SNX21
In Situ
Assay Products:
 

 
Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for SNX21

(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)
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This gene was present in the common ancestor of animals.

Orthologs for SNX21 gene from Selected 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 70.59(n)
62.65(a)
  419302  XM_417474.4  XP_417474.4 
tropical clawed frog
(Xenopus tropicalis)
Amphibia snx211 sorting nexin family member 21 54.94(n)
52.03(a)
  733824  NM_001045583.1  NP_001039048.1 
zebrafish
(Danio rerio)
Actinopterygii snx211 sorting nexin family member 21 52.45(n)
46.54(a)
  555580  NM_001077368.2  NP_001070836.1 
fruit fly
(Drosophila melanogaster)
Insecta CG30771 CG3077 44.93(n)
32.97(a)
  33466  NM_001273033.1  NP_001259962.1 


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)
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Paralogs for SNX21 gene
SNX202  
2 SIMAP similar genes for SNX21 using alignment to 4 protein entries:     SNX21_HUMAN (see all proteins):
C20orf161    SNX20

Find genes that share paralogs with SNX21           About GenesLikeMe



(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), the Human Cytochrome P450 Allele Nomenclature Database, and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers, Cancer Mutation PCR Arrays and Assays, and Copy Number PCR Arrays from QIAGEN)
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Selected SNPs for SNX21 (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

Site Specific Mutation Identification with 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, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
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  --

(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)
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PubMed articles for SNX21 gene, integrated from 10 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. (Biochem. Biophys. Res. Commun. 2002)
  2. Sorting out the cellular functions of sorting nexins. (PubMed id 12461558)1, 3 Worby C.A. and Dixon J.E. (Nat. Rev. Mol. Cell Biol. 2002)
  3. The DNA sequence and comparative analysis of human chromosome 20. (PubMed id 11780052)1, 2 Deloukas P....Rogers J. (Nature 2001)
  4. Toward an understanding of the protein interaction network of the human liver. (PubMed id 21988832)1 Wang J....Yang X. (Mol. Syst. Biol. 2011)
  5. Interactions of pathological hallmark proteins: tubulin polymerization promoting protein/p25, beta-amyloid, and alpha-synuclein. (PubMed id 21832049)1 OlA!h J....OvA!di J. (J. Biol. Chem. 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. (Genome Res. 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. (Genome Res. 2004)
  8. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1 Ota T.... Sugano S. (Nat. Genet. 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. (Proc. Natl. Acad. Sci. U.S.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. (Biochem. J. 2001)

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

(According to HUGE)
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  --

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL, and/or others, e.g. Wikipedia and GeneReviews, via UniProtKB/Swiss-Prot)
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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.)
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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



(Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, eBioscience, and/or others, Gene Editing from DNA2.0. Clones from OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Addgene, Cell lines from GenScript, and ESI BIO, Flow cytometery from eBioscience, PCR Arrays from QIAGEN, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, Enzo Life Sciences, and/or ApexBio, In Situ Hybridization Assays from
Advanced Cell Diagnostics, Animal models from inGenious Targeting Laboratory, genOway)
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