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Aliases for MIR4687 Gene

Subcategory (RNA class) for MIR4687 Gene

miRNA

Quality Score for this RNA gene is

3

Aliases for MIR4687 Gene

  • MicroRNA 4687 2 3
  • STIM1 4 5
  • Stromal Interaction Molecule 1 5
  • Hsa-Mir-4687 3
  • GOK 4

External Ids for MIR4687 Gene

Previous GeneCards Identifiers for MIR4687 Gene

  • GC11U901863
  • GC11P003887
  • GC11P003856
  • GC11P003857

Summaries for MIR4687 Gene

Entrez Gene Summary for MIR4687 Gene

  • microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]

GeneCards Summary for MIR4687 Gene

MIR4687 (MicroRNA 4687) is an RNA Gene, and is affiliated with the miRNA class. Diseases associated with MIR4687 include Stormorken Syndrome and Immunodeficiency 10. Among its related pathways are Immune System and Downstream signaling events of B Cell Receptor (BCR). An important paralog of this gene is STIM2.

UniProtKB/Swiss-Prot for MIR4687 Gene

  • Plays a role in mediating store-operated Ca(2+) entry (SOCE), a Ca(2+) influx following depletion of intracellular Ca(2+) stores (PubMed:15866891, PubMed:16005298, PubMed:16208375, PubMed:16537481, PubMed:16733527, PubMed:16766533, PubMed:16807233, PubMed:18854159, PubMed:19249086, PubMed:22464749, PubMed:24069340, PubMed:24351972, PubMed:24591628, PubMed:26322679, PubMed:25326555). Acts as Ca(2+) sensor in the endoplasmic reticulum via its EF-hand domain. Upon Ca(2+) depletion, translocates from the endoplasmic reticulum to the plasma membrane where it activates the Ca(2+) release-activated Ca(2+) (CRAC) channel subunit ORAI1 (PubMed:16208375, PubMed:16537481). Involved in enamel formation (PubMed:24621671). Activated following interaction with TMEM110/STIMATE, leading to promote STIM1 conformational switch (PubMed:26322679).

No data available for Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for MIR4687 Gene

Genomics for MIR4687 Gene

Regulatory Elements for MIR4687 Gene

Enhancers for MIR4687 Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH11F003875 1.6 FANTOM5 Ensembl ENCODE 14 +23.9 23874 6.8 HDGF PKNOX1 ARNT ARID4B FEZF1 DMAP1 YY1 GATA2 JUNB NCOA1 STIM1 RHOG RRM1 ENSG00000229368 LOC105376527 MIR4687 ENSG00000206976 ENSG00000230593 NUP98 OR52B4
GH11F003941 1.5 FANTOM5 Ensembl ENCODE 12.6 +94.5 94547 14.7 PKNOX1 ARNT YY1 ZNF121 GATA2 KLF13 NCOA1 MIER2 REST TBX21 STIM1 RRM1 ENSG00000206976 MIR4687 ENSG00000229368 LOC105376527 RHOG ENSG00000255232 GC11P003932
GH11F003900 1.3 Ensembl ENCODE 13.5 +50.0 49974 8.6 HDGF PKNOX1 ATF1 ZFP64 ARID4B SIN3A FEZF1 DMAP1 YY1 SP5 STIM1 RRM1 MIR4687 ENSG00000229368 LOC105376527 ENSG00000230593 GC11P003897 GC11P003920
GH11F003958 1.1 Ensembl ENCODE 12.6 +105.4 105374 3.0 THRB RAD21 GATA2 CREM CEBPB JUNB NR2F2 TFDP1 MAFF IKZF1 STIM1 RRM1 ENSG00000206976 MIR4687 LOC105376527 ENSG00000229368 RHOG ENSG00000255232 GC11P003932
GH11F004056 1.2 Ensembl ENCODE 11.4 +204.6 204577 4.3 TBP PKNOX1 ARID4B THRB ZSCAN9 RARA ETV6 CREM MIXL1 THAP11 RRM1 ENSG00000206976 MIR4687 STIM1 ENSG00000229368 LOC105376527 RPS29P20
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around MIR4687 on UCSC Golden Path with GeneCards custom track

Promoters for MIR4687 Gene
Ensembl Regulatory Elements (ENSRs) TSS Distance (bp) Size (bp) Binding Sites for Transcription Factors within promoters
ENSR00000317209 1573 3001 HDGF PKNOX1 ARNT ZFP64 ARID4B SIN3A DMAP1 ZNF2 YY1 ZNF207

Genomic Location for MIR4687 Gene

Chromosome:
11
Start:
3,854,527 bp from pter
End:
4,093,210 bp from pter
Size:
238,684 bases
Orientation:
Plus strand

Genomic View for MIR4687 Gene

Genes around MIR4687 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
MIR4687 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for MIR4687 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for MIR4687 Gene

Proteins for MIR4687 Gene

  • Protein details for MIR4687 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Q13586-STIM1_HUMAN
    Recommended name:
    Stromal interaction molecule 1
    Protein Accession:
    Q13586
    Secondary Accessions:
    • E9PQJ4
    • Q8N382

    Protein attributes for MIR4687 Gene

    Size:
    685 amino acids
    Molecular mass:
    77423 Da
    Quaternary structure:
    • Forms homooligomers and heterooligomers with STIM2 (PubMed:11463338, PubMed:11983428, PubMed:18854159, PubMed:22451904, PubMed:24351972, PubMed:24069340). Interacts (via the transmembrane region and the SOAR/CAD domain) with SPPL3; the interaction promotes the binding of STIM1 to ORAI1 (PubMed:25384971). Interacts with ORAI1 (PubMed:17905723, PubMed:19249086, PubMed:24351972). Interacts with MAPRE1; probably required for targeting to the growing microtubule plus ends (PubMed:19632184). Interacts with CRACR2A/EFCAB4B; the interaction is direct and takes place in absence of Ca(2+) (PubMed:20418871). Forms a complex with CRACR2A/EFCAB4B and ORAI1 at low concentration of Ca(2+), the complex dissociates at elevated Ca(2+) concentrations (PubMed:20418871). Interacts with SARAF, promoting a slow inactivation of STIM1-dependent SOCE activity, possibly by facilitating the deoligomerization of STIM1 (PubMed:22464749). Interacts with ASPH (isoform 8) (PubMed:22586105). Interacts with SLC35G1; intracellular Ca(2+)-dependent. May interact with ATP1A1, ATP2A2, ATP2B1, ATP2B4, KPNB1 and XPO1; through SLC35G1 (PubMed:22084111). Interacts with TMEM203 (PubMed:25996873). Interacts with TMEM110/STIMATE, promoting STIM1 conformational switch (PubMed:26322679). Interacts with TMEM178A (By similarity).
    • Forms homooligomers and heterooligomers with STIM2 (PubMed:11463338, PubMed:11983428, PubMed:18854159, PubMed:22451904, PubMed:24351972, PubMed:24069340). Interacts (via the transmembrane region and the SOAR/CAD domain) with SPPL3; the interaction promotes the binding of STIM1 to ORAI1 (PubMed:25384971). Interacts with ORAI1 (PubMed:17905723, PubMed:19249086, PubMed:24351972). Interacts with MAPRE1; probably required for targeting to the growing microtubule plus ends (PubMed:19632184). Interacts with CRACR2A/EFCAB4B; the interaction is direct and takes place in absence of Ca(2+) (PubMed:20418871). Forms a complex with CRACR2A/EFCAB4B and ORAI1 at low concentration of Ca(2+), the complex dissociates at elevated Ca(2+) concentrations (PubMed:20418871). Interacts with SARAF, promoting a slow inactivation of STIM1-dependent SOCE activity, possibly by facilitating the deoligomerization of STIM1 (PubMed:22464749). Interacts with ASPH (isoform 8) (PubMed:22586105). Interacts with SLC35G1; intracellular Ca(2+)-dependent. May interact with ATP1A1, ATP2A2, ATP2B1, ATP2B4, KPNB1 and XPO1; through SLC35G1 (PubMed:22084111). Interacts with TMEM203 (PubMed:25996873). Interacts with TMEM110/STIMATE, promoting STIM1 conformational switch (PubMed:26322679). Interacts with TMEM178A (By similarity).
    Miscellaneous:
    • Transfection of STIM1 into cells derived from a rhabdoid tumor and from a rhabdomyosarcoma that do not express detectable levels of STIM1 can induce cell death, suggesting a possible role in the control of rhabdomyosarcomas and rhabdoid tumors.

    Three dimensional structures from OCA and Proteopedia for MIR4687 Gene

    Alternative splice isoforms for MIR4687 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for MIR4687 Gene

Post-translational modifications for MIR4687 Gene

No data available for DME Specific Peptides for MIR4687 Gene

Domains & Families for MIR4687 Gene

Gene Families for MIR4687 Gene

Protein Domains for MIR4687 Gene

Graphical View of Domain Structure for InterPro Entry

Q13586

UniProtKB/Swiss-Prot:

STIM1_HUMAN :
  • The microtubule tip localization signal (MtLS) motif; mediates interaction with MAPRE1 and targeting to the growing microtubule plus ends.
Domain:
  • The microtubule tip localization signal (MtLS) motif; mediates interaction with MAPRE1 and targeting to the growing microtubule plus ends.
  • The STIM1 Orai1-activating region/CRAC-activating domain (SOAR/CAD) mediates interaction with ORAI1 to activate the channel.
  • Contains 1 EF-hand domain.
  • Contains 1 SAM (sterile alpha motif) domain.
genes like me logo Genes that share domains with MIR4687: view

No data available for Suggested Antigen Peptide Sequences for MIR4687 Gene

Function for MIR4687 Gene

Molecular function for MIR4687 Gene

UniProtKB/Swiss-Prot Function:
Plays a role in mediating store-operated Ca(2+) entry (SOCE), a Ca(2+) influx following depletion of intracellular Ca(2+) stores (PubMed:15866891, PubMed:16005298, PubMed:16208375, PubMed:16537481, PubMed:16733527, PubMed:16766533, PubMed:16807233, PubMed:18854159, PubMed:19249086, PubMed:22464749, PubMed:24069340, PubMed:24351972, PubMed:24591628, PubMed:26322679, PubMed:25326555). Acts as Ca(2+) sensor in the endoplasmic reticulum via its EF-hand domain. Upon Ca(2+) depletion, translocates from the endoplasmic reticulum to the plasma membrane where it activates the Ca(2+) release-activated Ca(2+) (CRAC) channel subunit ORAI1 (PubMed:16208375, PubMed:16537481). Involved in enamel formation (PubMed:24621671). Activated following interaction with TMEM110/STIMATE, leading to promote STIM1 conformational switch (PubMed:26322679).

Gene Ontology (GO) - Molecular Function for MIR4687 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005246 calcium channel regulator activity IEA --
GO:0005509 calcium ion binding IDA --
GO:0005515 protein binding IPI --
GO:0015279 store-operated calcium channel activity IEA --
GO:0042802 identical protein binding IPI --
genes like me logo Genes that share ontologies with MIR4687: view

Animal Model Products

miRNA Products

Clone Products

Flow Cytometry Products

No data available for Enzyme Numbers (IUBMB) , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for MIR4687 Gene

Localization for MIR4687 Gene

Subcellular locations from UniProtKB/Swiss-Prot for MIR4687 Gene

Cell membrane; Single-pass type I membrane protein. Endoplasmic reticulum membrane; Single-pass type I membrane protein. Cytoplasm, cytoskeleton. Sarcoplasmic reticulum. Note=Translocates from the endoplasmic reticulum to the cell membrane in response to a depletion of intracellular calcium and is detected at punctae corresponding to junctions between the endoplasmic reticulum and the cell membrane (PubMed:19249086, PubMed:16005298, PubMed:16208375, PubMed:18854159). Associated with the microtubule network at the growing distal tip of microtubules (PubMed:19632184). {ECO:0000269 PubMed:16005298, ECO:0000269 PubMed:16208375, ECO:0000269 PubMed:18854159, ECO:0000269 PubMed:19249086, ECO:0000269 PubMed:19632184}.

Gene Ontology (GO) - Cellular Components for MIR4687 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005737 cytoplasm IEA --
GO:0005783 endoplasmic reticulum IDA --
GO:0005789 endoplasmic reticulum membrane TAS --
GO:0005856 cytoskeleton IEA --
GO:0005874 microtubule IEA --
genes like me logo Genes that share ontologies with MIR4687: view

No data available for Subcellular locations from COMPARTMENTS for MIR4687 Gene

Pathways & Interactions for MIR4687 Gene

genes like me logo Genes that share pathways with MIR4687: view

Gene Ontology (GO) - Biological Process for MIR4687 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0002115 store-operated calcium entry IEA --
GO:0005513 detection of calcium ion IDA --
GO:0006810 transport IEA --
GO:0006811 ion transport IEA --
GO:0006812 cation transport IEA --
genes like me logo Genes that share ontologies with MIR4687: view

No data available for SIGNOR curated interactions for MIR4687 Gene

Transcripts for MIR4687 Gene

mRNA/cDNA for MIR4687 Gene

(21) Ensembl transcripts including schematic representations, and UCSC links where relevant :

miRNA Products

Clone Products

Flow Cytometry Products

Alternative Splicing Database (ASD) splice patterns (SP) for MIR4687 Gene

No ASD Table

Relevant External Links for MIR4687 Gene

GeneLoc Exon Structure for
MIR4687
ECgene alternative splicing isoforms for
MIR4687

Expression for MIR4687 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and SAGE for MIR4687 Gene

NURSA nuclear receptor signaling pathways regulating expression of MIR4687 Gene:

MIR4687

mRNA Expression by UniProt/SwissProt for MIR4687 Gene:

Q13586-STIM1_HUMAN
Tissue specificity: Ubiquitously expressed in various human primary cells and tumor cell lines.
genes like me logo Genes that share expression patterns with MIR4687: view

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression and Protein tissue co-expression partners for MIR4687 Gene

Orthologs for MIR4687 Gene

This gene was present in the common ancestor of animals.

Orthologs for MIR4687 Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia STIM1 35
  • 100 (a)
OneToOne
mouse
(Mus musculus)
Mammalia Stim1 35
  • 97 (a)
OneToOne
cow
(Bos Taurus)
Mammalia STIM1 35
  • 96 (a)
OneToOne
dog
(Canis familiaris)
Mammalia STIM1 35
  • 96 (a)
OneToOne
oppossum
(Monodelphis domestica)
Mammalia STIM1 35
  • 83 (a)
OneToOne
platypus
(Ornithorhynchus anatinus)
Mammalia STIM1 35
  • 72 (a)
OneToOne
chicken
(Gallus gallus)
Aves STIM1 35
  • 69 (a)
OneToOne
lizard
(Anolis carolinensis)
Reptilia STIM1 35
  • 71 (a)
OneToOne
zebrafish
(Danio rerio)
Actinopterygii stim1a 35
  • 61 (a)
OneToOne
fruit fly
(Drosophila melanogaster)
Insecta Stim 35
  • 32 (a)
OneToMany
worm
(Caenorhabditis elegans)
Secernentea stim-1 35
  • 26 (a)
OneToMany
Species where no ortholog for MIR4687 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African clawed frog (Xenopus laevis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rat (Rattus norvegicus)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • tropical clawed frog (Silurana tropicalis)
  • wheat (Triticum aestivum)

Evolution for MIR4687 Gene

ENSEMBL:
Gene Tree for MIR4687 (if available)
TreeFam:
Gene Tree for MIR4687 (if available)

Paralogs for MIR4687 Gene

Paralogs for MIR4687 Gene

genes like me logo Genes that share paralogs with MIR4687: view

Variants for MIR4687 Gene

Sequence variations from dbSNP and Humsavar for MIR4687 Gene

SNP ID Clin Chr 11 pos Sequence Context AA Info Type
rs150033189 Likely benign 3,856,384(+) GGGGC(C/G)AACTC downstream-variant-500B, upstream-variant-2KB, reference, synonymous-codon
rs10835206 -- 3,855,844(+) CTCGC(C/T)GCTCT upstream-variant-2KB, utr-variant-5-prime
rs111463845 -- 3,854,394(+) AATTC(A/G)TGTTC nc-transcript-variant, upstream-variant-2KB
rs112182691 -- 3,856,619(+) CATCC(C/G)CCGCA intron-variant, downstream-variant-500B, upstream-variant-2KB
rs112807206 -- 3,854,249(+) AGGTG(A/G)CTGAG downstream-variant-500B, upstream-variant-2KB

Relevant External Links for MIR4687 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for
MIR4687

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Structural Variations from Database of Genomic Variants (DGV) and Variation tolerance for MIR4687 Gene

Disorders for MIR4687 Gene

MalaCards: The human disease database

(4) MalaCards diseases for MIR4687 Gene - From: GeneCards

Disorder Aliases PubMed IDs
stormorken syndrome
  • thrombocytopathy, asplenia and miosis
immunodeficiency 10
  • immune dysfunction with t-cell inactivation due to calcium entry defect 2
iris hypoplasia
myopathy, tubular aggregate, 1
  • myeloproliferative syndrome, transient
- elite association - COSMIC cancer census association via MalaCards

UniProtKB/Swiss-Prot

STIM1_HUMAN
  • Immunodeficiency 10 (IMD10) [MIM:612783]: An immune disorder characterized by recurrent infections, impaired activation and proliferative response of T-cells, decreased T-cell production of cytokines, lymphadenopathy, and normal lymphocytes counts and serum immunoglobulin levels. Additional features include thrombocytopenia, autoimmune hemolytic anemia, myopathy, partial iris hypoplasia, hepatosplenomegaly and defective enamel dentition. {ECO:0000269 PubMed:19420366, ECO:0000269 PubMed:22190180}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Myopathy, tubular aggregate, 1 (TAM1) [MIM:160565]: A rare congenital myopathy characterized by regular arrays of membrane tubules on muscle biopsies without additional histopathological hallmarks. Tubular aggregates in muscle are structures of variable appearance consisting of an outer tubule containing either one or more microtubule-like structures or amorphous material. They may occur in a variety of circumstances, including inherited myopathies, alcohol- and drug-induced myopathies, exercise-induced cramps or muscle weakness. {ECO:0000269 PubMed:23332920, ECO:0000269 PubMed:24570283, ECO:0000269 PubMed:25326555, ECO:0000269 PubMed:25953320}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Stormorken syndrome (STRMK) [MIM:185070]: A rare autosomal dominant disease characterized by mild bleeding tendency, thrombocytopathy, thrombocytopenia, mild anemia, asplenia, tubular aggregate myopathy, miosis, headache, and ichthyosis. {ECO:0000269 PubMed:24591628, ECO:0000269 PubMed:24619930, ECO:0000269 PubMed:25577287}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Relevant External Links for MIR4687

Atlas of Genetics and Cytogenetics in Oncology and Haematology:
MIR4687
genes like me logo Genes that share disorders with MIR4687: view

No data available for Genatlas for MIR4687 Gene

Publications for MIR4687 Gene

  1. York platelet syndrome is a CRAC channelopathy due to gain-of- function mutations in STIM1. (PMID: 25577287) Markello T. … Gunay-Aygun M. (Mol. Genet. Metab. 2015) 4 64
  2. N-terminome analysis of the human mitochondrial proteome. (PMID: 25944712) Vaca Jacome A.S. … Carapito C. (Proteomics 2015) 4 64
  3. 50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutation. (PMID: 25953320) Walter M.C. … Schoser B. (Neuromuscul. Disord. 2015) 4 64
  4. TMEM203 is a novel regulator of intracellular calcium homeostasis and is required for spermatogenesis. (PMID: 25996873) Shambharkar P.B. … Labow M.A. (PLoS ONE 2015) 4 64
  5. Proteomic mapping of ER-PM junctions identifies STIMATE as a regulator of Ca(2+) influx. (PMID: 26322679) Jing J. … Zhou Y. (Nat. Cell Biol. 2015) 4 64

Products for MIR4687 Gene

Sources for MIR4687 Gene

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