This gene encodes a conserved zinc finger protein. The encoded protein functions in skin color saturation. Mutations in this gene are associated with facial pigmented spots. This gene is also associated with susceptibility to adolescent idiopathic scoliosis. [provided by RefSeq, Jul 2016] See more...

Aliases for BNC2 Gene

Aliases for BNC2 Gene

  • Basonuclin 2 2 3 5
  • Zinc Finger Protein Basonuclin-2 3 4
  • BSN2 2 3
  • FLJ20043 2
  • LUTO 3
  • BNC2 5

External Ids for BNC2 Gene

Previous GeneCards Identifiers for BNC2 Gene

  • GC09U900603

Summaries for BNC2 Gene

Entrez Gene Summary for BNC2 Gene

  • This gene encodes a conserved zinc finger protein. The encoded protein functions in skin color saturation. Mutations in this gene are associated with facial pigmented spots. This gene is also associated with susceptibility to adolescent idiopathic scoliosis. [provided by RefSeq, Jul 2016]

GeneCards Summary for BNC2 Gene

BNC2 (Basonuclin 2) is a Protein Coding gene. Diseases associated with BNC2 include Lower Urinary Tract Obstruction, Congenital and Urinary Tract Obstruction. An important paralog of this gene is BNC1.

UniProtKB/Swiss-Prot Summary for BNC2 Gene

  • Probable transcription factor specific for skin keratinocytes. May play a role in the differentiation of spermatozoa and oocytes (PubMed:14988505). May also play an important role in early urinary-tract development (PubMed:31051115).

Gene Wiki entry for BNC2 Gene

No data available for CIViC Summary , Tocris Summary , PharmGKB "VIP" Summary , Rfam classification and piRNA Summary for BNC2 Gene

Genomics for BNC2 Gene

GeneHancer (GH) Regulatory Elements Pubs

Promoters and enhancers for BNC2 Gene
GeneHancer (GH) Identifier GH Type GH
Score
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH09J016725 Promoter/Enhancer 2.4 UCNEbase EPDnew Ensembl ENCODE CraniofacialAtlas dbSUPER 250.1 +143.7 143742 3.8 ZNF600 ZNF10 POLR2A CEBPB ZNF341 MAX SIN3A RAD21 SMC3 TBP BNC2-AS1 BNC2 piR-57460-662
GH09J016866 Promoter/Enhancer 2.2 EPDnew FANTOM5 Ensembl ENCODE CraniofacialAtlas 262.1 +1.5 1545 6.6 ZNF600 POLR2A CEBPB FEZF1 ZNF341 SIN3A EP300 SP2 TCF7L2 ZBTB48 BNC2 hsa-miR-5096-142 FJ601678-135
GH09J016702 Promoter/Enhancer 2.2 UCNEbase EPDnew Ensembl ENCODE CraniofacialAtlas dbSUPER 250.1 +166.4 166373 4.8 ZNF600 JUND ZNF580 ATF2 POLR2A ZIC2 CEBPB DEK FEZF1 ZNF341 BNC2 lnc-CNTLN-6 HSALNG0070210 lnc-C9orf92-4
GH09J016680 Enhancer 1.3 UCNEbase Ensembl ENCODE CraniofacialAtlas dbSUPER 11.4 +189.0 189042 2.8 PRDM6 ZBTB48 ZNF398 GATA2 TRIM28 OSR2 ZBTB20 BNC2-AS1 BNC2 RF00017-6872 lnc-CNTLN-6 HSALNG0070210 lnc-C9orf92-4
GH09J016824 Enhancer 1.3 UCNEbase ENCODE CraniofacialAtlas dbSUPER 11.2 +45.1 45061 3.3 JUND CTCF RAD21 SMC3 BHLHE40 POLR2A RFX1 MZF1 EP300 FOS BNC2 ENSG00000230694 FJ601678-135
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around BNC2 on the GeneHancer Hub at the UCSC Golden Path

Cistromic (ChIP-Seq) regulation report from SPP (The Signaling Pathways Project) for BNC2

Top Transcription factor binding sites by QIAGEN in the BNC2 gene promoter:
  • AREB6
  • Cdc5
  • FOXD3
  • HFH-1
  • ISGF-3
  • Nkx2-5
  • Olf-1
  • RORalpha1
  • RP58
  • Sox5

Genomic Locations for BNC2 Gene

Latest Assembly
chr9:16,409,503-16,870,843
(GRCh38/hg38)
Size:
461,341 bases
Orientation:
Minus strand

Previous Assembly
chr9:16,409,501-16,870,668
(GRCh37/hg19 by Entrez Gene)
Size:
461,168 bases
Orientation:
Minus strand

chr9:16,409,501-16,870,841
(GRCh37/hg19 by Ensembl)
Size:
461,341 bases
Orientation:
Minus strand

Genomic View for BNC2 Gene

Genes around BNC2 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
BNC2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for BNC2 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for BNC2 Gene

Proteins for BNC2 Gene

  • Protein details for BNC2 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Q6ZN30-BNC2_HUMAN
    Recommended name:
    Zinc finger protein basonuclin-2
    Protein Accession:
    Q6ZN30
    Secondary Accessions:
    • B1APG9
    • Q6T3A3
    • Q8NAR2
    • Q9H6J0
    • Q9NXV0

    Protein attributes for BNC2 Gene

    Size:
    1099 amino acids
    Molecular mass:
    122330 Da
    Quaternary structure:
    No Data Available
    SequenceCaution:
    • Sequence=AAR99389.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305}; Sequence=BAA90908.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305}; Sequence=BAB15269.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305}; Sequence=BAC03837.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305};

    Alternative splice isoforms for BNC2 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for BNC2 Gene

Post-translational modifications for BNC2 Gene

  • Modification sites at PhosphoSitePlus
  • Modification sites at neXtProt

No data available for DME Specific Peptides for BNC2 Gene

Domains & Families for BNC2 Gene

Gene Families for BNC2 Gene

HGNC:
Human Protein Atlas (HPA):
  • Predicted intracellular proteins
  • Transcription factors

Protein Domains for BNC2 Gene

Suggested Antigen Peptide Sequences for BNC2 Gene

GenScript: Design optimal peptide antigens:
  • cDNA FLJ58670, highly similar to Zinc finger protein basonuclin-2 (B4E3J2_HUMAN)
  • Zinc finger protein basonuclin-2 (BNC2_HUMAN)
  • Basonuclin 2 (Q06HB5_HUMAN)
  • Basonuclin 2 (Q06HB6_HUMAN)
  • Basonuclin 2 (Q06HB7_HUMAN)
genes like me logo Genes that share domains with BNC2: view

No data available for Graphical View of Domain Structure and UniProtKB/Swiss-Prot for BNC2 Gene

Function for BNC2 Gene

Molecular function for BNC2 Gene

UniProtKB/Swiss-Prot Function:
Probable transcription factor specific for skin keratinocytes. May play a role in the differentiation of spermatozoa and oocytes (PubMed:14988505). May also play an important role in early urinary-tract development (PubMed:31051115).

Phenotypes From GWAS Catalog for BNC2 Gene

Gene Ontology (GO) - Molecular Function for BNC2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000976 transcription regulatory region sequence-specific DNA binding IBA 21873635
GO:0003677 DNA binding IEA --
GO:0005515 protein binding IPI 32296183
GO:0008270 zinc ion binding IEA --
GO:0046872 metal ion binding IEA --
genes like me logo Genes that share ontologies with BNC2: view
genes like me logo Genes that share phenotypes with BNC2: view

Human Phenotype Ontology for BNC2 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for BNC2 Gene

MGI Knock Outs for BNC2:
  • Bnc2 Bnc2<tm1b(KOMP)Wtsi>

miRNA for BNC2 Gene

miRTarBase miRNAs that target BNC2

Inhibitory RNAs for research

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for BNC2

No data available for Enzyme Numbers (IUBMB) , Transcription Factor Targets and HOMER Transcription for BNC2 Gene

Localization for BNC2 Gene

Subcellular locations from UniProtKB/Swiss-Prot for BNC2 Gene

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for BNC2 gene
Compartment Confidence
nucleus 5
plasma membrane 2
cytosol 2
extracellular 1
cytoskeleton 1
mitochondrion 1

Subcellular locations from the

Human Protein Atlas (HPA)

Gene Ontology (GO) - Cellular Components for BNC2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005634 nucleus IEA,IBA 21873635
GO:0005654 nucleoplasm IDA --
genes like me logo Genes that share ontologies with BNC2: view

Pathways & Interactions for BNC2 Gene

PathCards logo

SuperPathways for BNC2 Gene

No Data Available

Gene Ontology (GO) - Biological Process for BNC2 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0003416 endochondral bone growth IEA --
GO:0006355 regulation of transcription, DNA-templated IBA 21873635
GO:0043586 tongue development IEA --
GO:0060021 roof of mouth development IEA --
GO:0060485 mesenchyme development IEA --
genes like me logo Genes that share ontologies with BNC2: view

No data available for Pathways by source and SIGNOR curated interactions for BNC2 Gene

Drugs & Compounds for BNC2 Gene

No Compound Related Data Available

Transcripts for BNC2 Gene

mRNA/cDNA for BNC2 Gene

3 REFSEQ mRNAs :
28 NCBI additional mRNA sequence :
14 Ensembl transcripts including schematic representations, and UCSC links to gene/alias where relevant :

Inhibitory RNAs for research

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for BNC2

Alternative Splicing Database (ASD) splice patterns (SP) for BNC2 Gene

ExUns: 1 ^ 2 ^ 3a · 3b ^ 4 ^ 5 ^ 6a · 6b ^ 7 ^ 8 ^ 9a · 9b · 9c ^ 10 ^ 11 ^ 12
SP1: - - - - - -
SP2: -
SP3:
SP4:
SP5:
SP6:

Relevant External Links for BNC2 Gene

GeneLoc Exon Structure for
BNC2

Expression for BNC2 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and SAGE for BNC2 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for BNC2 Gene

This gene is overexpressed in Uterus (x5.6), Ovary (x5.6), and Fallopian Tube (x4.9).

Protein differential expression in normal tissues from HIPED for BNC2 Gene

This gene is overexpressed in Vitreous humor (65.7).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB and MOPED for BNC2 Gene



Protein tissue co-expression partners for BNC2 Gene

Transcriptomic regulation report from SPP (The Signaling Pathways Project) for BNC2

SOURCE GeneReport for Unigene cluster for BNC2 Gene:

Hs.656581

mRNA Expression by UniProt/SwissProt for BNC2 Gene:

Q6ZN30-BNC2_HUMAN
Tissue specificity: Highly expressed in testis, uterus and small intestine, and weakly expressed in colon and prostate. Also expressed in skin, primary keratinocytes, immortalized keratinocytes, and HeLa and HEK293 cells. Not detected in blood, thymus, spleen or Hep-G2 cells.

Evidence on tissue expression from TISSUES for BNC2 Gene

  • Muscle(3.1)
  • Skin(2)
genes like me logo Genes that share expression patterns with BNC2: view

Primer products for research

No data available for Phenotype-based relationships between genes and organs from Gene ORGANizer for BNC2 Gene

Orthologs for BNC2 Gene

This gene was present in the common ancestor of animals.

Orthologs for BNC2 Gene

Organism Taxonomy Gene Similarity Type Details
Chimpanzee
(Pan troglodytes)
Mammalia BNC2 29 30
  • 99.82 (n)
OneToOne
Dog
(Canis familiaris)
Mammalia BNC2 29 30
  • 94.29 (n)
OneToOne
Platypus
(Ornithorhynchus anatinus)
Mammalia BNC2 30
  • 93 (a)
OneToOne
Oppossum
(Monodelphis domestica)
Mammalia BNC2 30
  • 92 (a)
OneToOne
Cow
(Bos Taurus)
Mammalia BNC2 29 30
  • 91.96 (n)
OneToOne
Rat
(Rattus norvegicus)
Mammalia Bnc2 29
  • 90.99 (n)
Mouse
(Mus musculus)
Mammalia Bnc2 29 16 30
  • 90.91 (n)
OneToOne
Chicken
(Gallus gallus)
Aves BNC2 29 30
  • 83.41 (n)
OneToOne
Lizard
(Anolis carolinensis)
Reptilia BNC2 30
  • 62 (a)
OneToOne
Tropical Clawed Frog
(Silurana tropicalis)
Amphibia bnc2 29
  • 76.94 (n)
Zebrafish
(Danio rerio)
Actinopterygii bnc2 30
  • 61 (a)
OneToOne
Fruit Fly
(Drosophila melanogaster)
Insecta disco 30
  • 25 (a)
ManyToMany
disco-r 30
  • 13 (a)
ManyToMany
Worm
(Caenorhabditis elegans)
Secernentea F55C5.11 30
  • 33 (a)
OneToMany
Species where no ortholog for BNC2 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Eremothecium 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)
  • Rice (Oryza sativa)
  • Rice Blast Fungus (Magnaporthe grisea)
  • Schistosome Parasite (Schistosoma mansoni)
  • Sea Anemone (Nematostella vectensis)
  • Sea Vase (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)
  • Wheat (Triticum aestivum)

Evolution for BNC2 Gene

ENSEMBL:
Gene Tree for BNC2 (if available)
TreeFam:
Gene Tree for BNC2 (if available)
Aminode:
Evolutionary constrained regions (ECRs) for BNC2: view image
Alliance of Genome Resources:
Additional Orthologs for BNC2

Paralogs for BNC2 Gene

Paralogs for BNC2 Gene

(7) SIMAP similar genes for BNC2 Gene using alignment to 22 proteins:

  • BNC2_HUMAN
  • B1APH0_HUMAN
  • F5H586_HUMAN
  • H0Y4J1_HUMAN
  • H0Y6W5_HUMAN
  • Q06HB5_HUMAN
  • Q06HB6_HUMAN
  • Q06HB7_HUMAN
  • Q06HB8_HUMAN
  • Q06HB9_HUMAN
  • Q06HC0_HUMAN
  • Q06HC1_HUMAN
  • Q06HC2_HUMAN
  • Q06HC3_HUMAN
  • Q06HC4_HUMAN
  • Q06HC5_HUMAN
  • Q06HC6_HUMAN
  • Q06HC7_HUMAN
  • S4R351_HUMAN
  • S4R3K9_HUMAN
  • S4R3R8_HUMAN
  • S4R3X5_HUMAN
genes like me logo Genes that share paralogs with BNC2: view

Variants for BNC2 Gene

Sequence variations, with clinical significance, from ClinVar and Humsavar, with links to dbSNP for BNC2 Gene

SNP ID Clinical significance and condition Chr 09 pos Variation AA Info Type
870151 Benign: Amelogenesis imperfecta 16,419,429(-) C/T
NM_017637.6(BNC2):c.2860G>A (p.Ala954Thr)
MISSENSE_VARIANT,THREE_PRIME_UTR
rs114596065 Benign: Hypotension; not specified 16,436,326(-) G/T
NM_017637.6(BNC2):c.1868C>A (p.Pro623His)
MISSENSE
rs114612810 Benign: not provided 16,738,391(-) G/A
NM_017637.6(BNC2):c.98C>T (p.Pro33Leu)
MISSENSE_VARIANT,INTRON
rs114964332 Not Provided: Hypotension 16,437,278(-) G/C
NM_017637.6(BNC2):c.916C>G (p.Pro306Ala)
MISSENSE
rs116528562 Benign: not provided 16,436,377(-) G/A
NM_017637.6(BNC2):c.1817C>T (p.Pro606Leu)
MISSENSE

dbSNP identifiers (rs#s) for variants without ClinVar clinical significance for BNC2 Gene

All consequence types are included: molecular consequences (e.g. missense, synonymous), and location-based (e.g. intron, upstream).

Structural Variations from Database of Genomic Variants (DGV) for BNC2 Gene

Variant ID Type Subtype PubMed ID
dgv2137e212 CNV loss 25503493
dgv2138e212 CNV gain 25503493
dgv262n6 CNV deletion 16902084
esv1256705 CNV insertion 17803354
esv1359645 CNV insertion 17803354
esv1378850 CNV deletion 17803354
esv1725129 CNV deletion 17803354
esv2675274 CNV deletion 23128226
esv2738238 CNV deletion 23290073
esv2738240 CNV deletion 23290073
esv2738241 CNV deletion 23290073
esv2759673 CNV loss 17122850
esv2761269 CNV loss 21179565
esv3303408 CNV mobile element insertion 20981092
esv3308537 CNV mobile element insertion 20981092
esv3325173 CNV insertion 20981092
esv3344588 CNV insertion 20981092
esv3357139 CNV insertion 20981092
esv3401243 CNV insertion 20981092
esv3409571 CNV insertion 20981092
esv3437436 CNV insertion 20981092
esv3544602 CNV deletion 23714750
esv3573152 CNV loss 25503493
esv3573154 CNV loss 25503493
esv3619815 CNV loss 21293372
esv3619816 CNV loss 21293372
esv3619817 CNV gain 21293372
esv3619818 CNV loss 21293372
esv3619821 CNV loss 21293372
esv3619822 CNV loss 21293372
esv3891623 CNV gain 25118596
esv993349 CNV deletion 20482838
nsv1028923 CNV loss 25217958
nsv1030598 CNV loss 25217958
nsv1075194 CNV deletion 25765185
nsv1077093 CNV deletion 25765185
nsv1124402 CNV deletion 24896259
nsv1137426 CNV deletion 24896259
nsv1145207 CNV deletion 24896259
nsv466265 CNV loss 19166990
nsv476796 CNV novel sequence insertion 20440878
nsv510183 OTHER sequence alteration 20534489
nsv518608 CNV loss 19592680
nsv524264 CNV gain 19592680
nsv524954 CNV loss 19592680
nsv528443 CNV loss 19592680
nsv613670 CNV loss 21841781
nsv613671 CNV loss 21841781
nsv824866 CNV loss 20364138

Variation tolerance for BNC2 Gene

Residual Variation Intolerance Score: 10.7% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 4.19; 61.92% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for BNC2 Gene

Human Gene Mutation Database (HGMD)
BNC2
SNPedia medical, phenotypic, and genealogical associations of SNPs for
BNC2
Leiden Open Variation Database (LOVD)
BNC2

SNP Genotyping and Copy Number Assays for research

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for BNC2 Gene

Disorders for BNC2 Gene

MalaCards: The human disease database

(8) MalaCards diseases for BNC2 Gene - From: OMI, CVR, ORP, SWI, COP, and GCD

Disorder Aliases PubMed IDs
lower urinary tract obstruction, congenital
  • luto
urinary tract obstruction
  • obstructive uropathy
idiopathic scoliosis
  • scoliosis idiopathic
posterior urethral valves
  • congenital posterior urethral valves
scoliosis
- elite association - COSMIC cancer census association via MalaCards
Search BNC2 in MalaCards View complete list of genes associated with diseases

UniProtKB/Swiss-Prot

BNC2_HUMAN
  • Lower urinary tract obstruction, congenital (LUTO) [MIM:618612]: A disorder characterized by urinary bladder outflow obstruction, which can represent an anatomical blockage or a functional obstruction. The most common anatomical causes are posterior urethral valves at the level of the prostatic urethra, a lesion unique to males. Less common are anterior urethral valves, also called urethral atresia, that can occur in either sex. LUTO is an autosomal dominant disease with variable expression. {ECO:0000269 PubMed:31051115}. Note=The disease is caused by variants affecting the gene represented in this entry.

Additional Disease Information for BNC2

Human Genome Epidemiology Navigator
(HuGE)
Atlas
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
Open Targets Platform
Open Targets Platform
genes like me logo Genes that share disorders with BNC2: view

No data available for Genatlas for BNC2 Gene

Publications for BNC2 Gene

  1. Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction. (PMID: 31051115) Kolvenbach CM … Hilger AC (American journal of human genetics 2019) 3 4 72
  2. Basonuclin 2: an extremely conserved homolog of the zinc finger protein basonuclin. (PMID: 14988505) Vanhoutteghem A … Djian P (Proceedings of the National Academy of Sciences of the United States of America 2004) 3 4 22
  3. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PMID: 14702039) Ota T … Sugano S (Nature genetics 2004) 2 3 4
  4. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PMID: 20379614) Rose JE … Uhl GR (Molecular medicine (Cambridge, Mass.) 2010) 3 40
  5. Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. (PMID: 20628086) Bailey SD … DREAM investigators (Diabetes care 2010) 3 40

Products for BNC2 Gene

Sources for BNC2 Gene