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

SLC38A5 Gene

protein-coding   GIFtS: 52
GCID: GC0XM048317

solute carrier family 38, member 5
 Explore 2 diseases affiliated with
SLC38A5 via
MalaCards
our new
 Human Malady Compendium 
Biological research products
for SLC38A5    

Aliases
for SLC38A5 gene

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section
Aliases
Solute Carrier Family 38, Member 51 2     SNAT52 3
SN21 2 3 5     Pp71941
JM241 2 3     Sodium-Coupled Neutral Amino Acid Transporter 52
System N Transporter 22 3     Solute Carrier Family 38 Member 53

External Ids:    HGNC: 180701   Entrez Gene: 927452   Ensembl: ENSG000000174837   OMIM: 3006495   UniProtKB: Q8WUX13   

Export aliases for SLC38A5 gene to outside databases

Previous GC identifers: GC0XM047119 GC0XM046577 GC0XM047143 GC0XM047362 GC0XM048073 GC0XM048201 GC0XM045981


Summaries
for SLC38A5 gene

(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 SLC38A5:
The protein encoded by this gene is a system N sodium-coupled amino acid transporter involved in the transfer of
glutamine, asparagine, histidine, serine, alanine, and glycine. The encoded protein does not transport charged amino
acids, imino acids, or N-alkylated amino acids. This transporter is not inhibited by lithium.(provided by RefSeq, Jun
2010)

UniProtKB/Swiss-Prot: S38A5_HUMAN, Q8WUX1
Function: Functions as a sodium-dependent amino acid transporter which countertransport protons. Mediates the
saturable, pH-sensitive, and electrogenic cotransport of several neutral amino acids including glycine, asparagine,
alanine, serine, glutamine and histidine with sodium




Genomic Views
for SLC38A5 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 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000023.10  NC_018934.1  NT_079573.4  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SLC38A5 gene promoter:
         E2F-3a   E2F-4   CREB   p53   deltaCREB   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmid: SLC38A5 promoter sequence
   Search SABiosciences Chromatin IP Primers for SLC38A5

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SLC38A5


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

Entrez Gene cytogenetic band: Xp11.23   Ensembl cytogenetic band:  Xp11.23   HGNC cytogenetic band: Xp11.23

SLC38A5 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SLC38A5 gene location

GeneLoc information about chromosome X         GeneLoc Exon Structure

GeneLoc location for GC0XM048317:  view genomic region     (about GC identifiers)

Start:
 48,316,920 bp from pter      End:
 48,328,644 bp from pter
Size:
 11,725 bases      Orientation:
 minus strand

Proteins
for SLC38A5 gene

(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: S38A5_HUMAN, Q8WUX1 (See protein sequence)
Recommended Name: Sodium-coupled neutral amino acid transporter 5  
Size: 472 amino acids; 51457 Da
Subcellular location: Cell membrane; Multi-pass membrane protein (By similarity)
Sequence caution: Sequence=AAL55865.1; Type=Frameshift; Positions=161, 466;
Secondary accessions: B3KT20 B5MDE6 B7WPJ9 Q6PIW9 Q8WYU2 Q96PQ4
Alternative splicing: 2 isoforms:  Q8WUX1-1   Q8WUX1-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for SLC38A5: NX_Q8WUX1

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_Q8WUX1

    • SLC38A5 Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_277053.2  
    ENSEMBL proteins: 
     ENSP00000366073   ENSP00000366071   ENSP00000402988   ENSP00000407258   ENSP00000403976  
     ENSP00000389644   ENSP00000416948   ENSP00000313740  
    Reactome Protein details: Q8WUX1
    Human Recombinant Protein Products: 
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    Browse Sino Biological Recombinant Proteins
    Browse ProSpec Recombinant Proteins
    Uscn Proteins for SLC38A5

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

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005886plasma membrane TAS--
    GO:0016021integral to membrane IEA--


    SLC38A5 for ontologies           About GeneDecksing



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    Uscn ELISAs and CLIAs for SLC38A5

    Protein Domains /
    Families
    for SLC38A5 gene

    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    SLC38A5 for domains           About GeneDecksing

    1 InterPro domain/family:
     IPR013057 AA_transpt_TM

    Graphical View of Domain Structure for InterPro Entry Q8WUX1

    ProtoNet protein and cluster: Q8WUX1

    UniProtKB/Swiss-Prot: S38A5_HUMAN, Q8WUX1
    Similarity: Belongs to the amino acid/polyamine transporter 2 family


    Function
    for SLC38A5 gene

    (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
    Function Summary:

         UniProtKB/Swiss-Prot: S38A5_HUMAN, Q8WUX1
    Function: Functions as a sodium-dependent amino acid transporter which countertransport protons. Mediates the
    saturable, pH-sensitive, and electrogenic cotransport of several neutral amino acids including glycine, asparagine,
    alanine, serine, glutamine and histidine with sodium
    Enzyme regulation: Not inhibited by lithium
    Biophysicochemical properties: Kinetic parameters: KM=0.6 mM for histidine (at pH 8.0);

    miRNA
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    1 QIAGEN miScript miRNA Assays for microRNA that regulate SLC38A5:
    hsa-miR-3150a-3p
    SwitchGear 3'UTR luciferase reporter plasmid: SLC38A5 3' UTR sequence
    Inhib. RNA
    Products:            		Browse for Gene Knock-down Tools from EMD Millipore
    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for SLC38A5 (see all 7)
    OriGene shRNA RFP: SLC38A5
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    Gene Editing
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    Clone
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    Cell Line
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    In Situ Assay
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    Gene Ontology (GO): 3 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0015171amino acid transmembrane transporter activity ----
    GO:0015175neutral amino acid transmembrane transporter activity ----
    GO:0015187glycine transmembrane transporter activity IEA--


    SLC38A5 for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for SLC38A5:
     Decreased nuclei size in G2M 


    Pathways & Interactions
    for SLC38A5 gene

    (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

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Amino acid and oligopeptide SLC transporters
    		Amino acid and oligopeptide SLC transporters1.00
    		Transport of inorganic cations/anions and amino acids/oligopeptides0.52
    		Amino acid transport across the plasma membrane0.63
    2SLC-mediated transmembrane transport
    		SLC-mediated transmembrane transport1.00
    		Transmembrane transport of small molecules0.50

    Pathway sources
    See GeneCards unified pathways
    Show all pathways


    5        Reactome Pathways for SLC38A5
        SLC-mediated transmembrane transport
    Transmembrane transport of small molecules
    Amino acid and oligopeptide SLC transporters
    Amino acid transport across the plasma membrane
    Transport of inorganic cations/anions and amino acids/oligopeptides



    SLC38A5 for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for SLC38A5

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

    1 Interacting protein for SLC38A5 (ENSP000003137404) via UniProtKB, MINT, STRING, and/or I2D
    InteractantInteraction Details
    GeneCardExternal ID(s)
    UBCENSP000003448184STRING: ENSP00000344818
    About this table

    Gene Ontology (GO): 5/6 biological process terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003333amino acid transmembrane transport ----
    GO:0006811ion transport TAS--
    GO:0006865amino acid transport TAS--
    GO:0015804neutral amino acid transport ----
    GO:0015816glycine transport ----


    SLC38A5 for ontologies           About GeneDecksing



    Drugs & Compounds
    for SLC38A5 gene

    (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 SLC38A5

    1 HMDB Compound for SLC38A5    About this table
    CompoundSynonyms CAS #PubMed Ids
    SodiumSodium (see all 2)7440-23-5--
    Search CenterWatch for drugs/clinical trials and news about SLC38A5 / S38A5 

    Transcripts
    for SLC38A5 gene

    (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,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    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 SLC38A5 gene: 
    NM_033518.2  

    Unigene Cluster for SLC38A5:

    Solute carrier family 38, member 5
    Hs.195155  [show with all ESTs]
    Unigene Representative Sequence: AF276889
    13 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000376876 ENST00000376875(uc004djk.4) ENST00000497336 ENST00000462359
    ENST00000480105 ENST00000494034 ENST00000440085 ENST00000441948 ENST00000413668
    ENST00000416711 ENST00000488083 ENST00000429543 ENST00000317669(uc010nid.3)


    miRNA
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    1 QIAGEN miScript miRNA Assays for microRNA that regulate SLC38A5:
    hsa-miR-3150a-3p
    SwitchGear 3'UTR luciferase reporter plasmid: SLC38A5 3' UTR sequence
    Inhib. RNA
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    OriGene shRNA RFP: SLC38A5
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    Clone
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    Primer
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat SLC38A5
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat SLC38A5

    Additional cDNA sequence: 

    AF276889.1 AK094788.1 BC019246.2 BC027721.2 

    12 DOTS entries:

    DT.425866  DT.91761993  DT.91761987  DT.95167171  DT.95167165  DT.95167169  DT.121278348  DT.95167164 
    DT.121278336  DT.95167170  DT.95368883  DT.95167163 

    24/146 AceView cDNA sequences (see all 146):

    BM728577 BM141814 BU154264 BX098636 BF734846 BU627635 AA612723 BC027721 
    R16124 BE151973 BM926518 AK094788 BC019246 BU677924 AA714176 BE272907 
    BQ053504 BU187175 BX443861 AA149754 T31698 BI224629 AA149673 BE151978 

    GeneLoc Exon Structure


    Expression
    for SLC38A5 gene

    (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

    SLC38A5 expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GGAGGAGGAG

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

    SLC38A5 expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    2 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    PancreasDorsal Pancreatic BudImmature Beta Progenitor CellsPancreas
    PancreasVentral Pancreatic BudImmature Beta Progenitor CellsPancreas
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 3 LifeMap Cells 
    NameCategory
    Adult human kidney epithelial cells (Primary Cell)Kidney
    Mature brain microvascular endothelial cells (Derivation of blood-...)
    Definitive endoderm-like cells (A scalable, suspensi...)

    See SLC38A5 Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SLC38A5

    SOURCE GeneReport for Unigene cluster: Hs.195155

    UniProtKB/Swiss-Prot: S38A5_HUMAN, Q8WUX1
    Tissue specificity: Predominantly expressed in stomach, brain, liver, lung and intestinal tract

        SABiosciences Expression via Pathway-Focused PCR Arrays including SLC38A5: 
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              Drug Transporters in human mouse rat

    Primer
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    In Situ
    Assay Products:     
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    Orthologs
    for SLC38A5 gene

    (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 eukaryotes.

    Orthologs for SLC38A5 gene from 4/16 species (see all 16)    About this table
    Organism Taxonomic
    classification    		 Gene Description Human
    Similarity    		 Orthology
    Type    		 Details
    lizard
    (Anolis carolinensis)    		 Reptilia SLC38A56
    		 --
    		 69(a)
    		 1 ↔ 1
    		 2(69442765-69461873)
    zebrafish
    (Danio rerio)    		 Actinopterygii slc38a36
    si:dkey-48j7.56
    		 si:dkey-48j7.5
    		 63(a)
    57(a)
    		 1 ↔ many
    1 ↔ many
    		 8(24432917-24465405)
    8(26468724-26478746)
    thale cress
    (Arabidopsis thaliana)    		 eudicotyledons AT3G303906
    AT3G562006
    (see all 5)    		 transmembrane amino acid transporter-like protein
    (see all 5)    		 20(a)
    20(a)
    (see all 5)    		 many ↔ many
    many ↔ many
    (see all 5)    		 3(11976837-11979621)
    3(20850029-20852027)
    rice
    (Oryza sativa)    		 Liliopsida --
    --
    (see all 7)    		 amino acid transporter, putative, expressed
    (see all 7)    		 21(a)
    21(a)
    (see all 7)    		 many ↔ many
    many ↔ many
    (see all 7)    		 6(9395131-9398131)
    6(25689100-25692911)


    ENSEMBL Gene Tree for SLC38A5 (if available)
    TreeFam Gene Tree for SLC38A5 (if available) 

    Paralogs
    for SLC38A5 gene

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SLC38A5 gene
    SLC38A42  SLC38A62  SLC38A12  SLC38A22  SLC38A112  SLC38A102  
    5 SIMAP similar genes for SLC38A5 using alignment to 6 protein entries:     S38A5_HUMAN (see all proteins):
    SLC38A3    SLC38A6    SLC38A1    SLC38A2    SLC38A4

    SLC38A5 for paralogs           About GeneDecksing



    Genomic Variants
    for SLC38A5 gene

    (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

    10/183 NCBI SNPs in SLC38A5 are shown (see all 183)     About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance    		Chr X posSequence#AA
    Chg    		TypeMore#Allele
    freq    		PopTotal
    sample    		More
    ----------
    rs1927534831,2
    		--48316452(+) CCGAGA/TGAATG 1 -- int10--------
    rs1851338991,2
    		--48316499(+) CTCTGC/TCGCCC 1 -- int10--------
    rs44802431,2
    		C,--48316559(+) TGGGTC/TCAAGC 1 -- int13Minor allele frequency- T:0.00NA 5
    rs1429490461,2
    		--48316573(+) TCTCCC/TGCCTT 1 -- int10--------
    rs1900133011,2
    		--48316597(+) GCTGGA/GACTAT 1 -- int10--------
    rs1474597101,2
    		--48316623(+) ACCCAA/GTTAAT 1 -- int10--------
    rs59066701,2
    		C,F,H,--48316843(+) CACTCA/GCAGGG 1 -- int116Minor allele frequency- G:0.92NS EA NA 2120
    rs1428825221,2
    		--48317211(+) AACCAC/TGTTCA 1 -- ut310--------
    rs1506488361,2
    		C,--48317285(+) ATGTGC/TATGCG 1 -- ut310--------
    rs172811881,2
    		C,F,H,--48317386(+) CGGCCA/GTGAAG 2 T M mis128Minor allele frequency- G:0.06NA NS EA 7132

    HapMap Linkage Disequilibrium report for SLC38A5 (48316920 - 48328644 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 1 variation for SLC38A5
         1 CNV: 7789
    Locus Specific Mutation Databases (LSDB): SLC38A5

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    Disorders / Diseases
    for SLC38A5 gene

    (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
    SLC38A5 for disorders           About GeneDecksing

    OMIM gene information: 300649    OMIM disorders: --

    2 diseases for SLC38A5:    About MalaCards
    exudative vitreoretinopathy    vitreoretinopathy


    Export disorders for SLC38A5 gene to outside databases

    Publications
    for SLC38A5 gene

    (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 SLC38A5 gene, integrated from 9 sources (see all 15):
    (articles sorted by number of sources associating them with SLC38A5)    		    Utopia: connect your pdf to the dynamic
    world of online information

    1. Structure, function, and tissue expression pattern of human SN2, a subtype of the amino acid transport system N. (PubMed id 11243884)1, 2, 3 Nakanishi T.... Ganapathy V. (2001)
    2. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PubMed id 14702039)1, 2 Ota T.... Sugano S. (2004)
    3. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    4. Systematic and quantitative assessment of the ubiquiti n-modified proteome. (PubMed id 21906983)1 Kim W....Gygi S.P. (2011)
    5. A data set of human endogenous protein ubiquitination sites. (PubMed id 20972266)1 Shi Y....Qin J. (2011)
    6. Ubiquitin ligase substrate identification through qua ntitative proteomics at both the protein and peptide levels. (PubMed id 21987572)1 Lee K.A....Doedens J.R. (2011)
    7. A proteome-wide, quantitative survey of in vivo ubiqui tylation sites reveals widespread regulatory roles. (PubMed id 21890473)1 Wagner S.A....Choudhary C. (2011)
    8. Amino acid transport across mammalian intestinal and renal epithelia. (PubMed id 18195088)1 BrAPer S. (2008)
    9. Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non- syndromic mental retardation due to a microdeletion in an unstable genomic region. (PubMed id 17333282)1 Froyen G.... Turner G. (2007)
    10. 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)

    External Searches for SLC38A5 gene

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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    Genome Databases showing SLC38A5 gene

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 92745 HGNC: 18070 AceView: SLC38A5 Ensembl:ENSG00000017483 euGenes: HUgn92745
    ECgene: SLC38A5 H-InvDB: SLC38A5

    Other Databases showing SLC38A5 gene

    (According to HUGE)
    About This Section
    		   --

    Specialized Databases showing SLC38A5 gene

    (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 SLC38A5 Pharmacogenomics, SNPs, Pathways

    Intellectual Property
    for SLC38A5 gene

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    		Patent Information for SLC38A5 gene:
    Search GeneIP for patents involving SLC38A5

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



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