BORCS8-MEF2B cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	BORCS8-MEF2B
Entrez Gene ID	4207
Full Name	BORCS8-MEF2B readthrough
Synonyms	LOC729991-MEF2B,MEF2B,MEF2BNB-MEF2B
General protein information	Preferred Names BORCS8-MEF2B readthrough Names myocyte enhancer factor 2B LOC729991-MEF2B readthrough MEF2BNB-MEF2B readthrough
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 19 Map Location: 19p13.11
Summary	This gene represents numerous read-through transcripts that span GeneID:729991 and 100271849. Many read-through transcripts are predicted to be nonsense-mediated decay (NMD) candidates, and are thought to be non-coding. Some transcripts are predicted to be capable of translation reinitiation at a downstream AUG, resulting in expression of at least one isoform of myocyte enhancer factor 2B (MEF2B) from this read-through locus. At least one additional MEF2B variant and isoform can be expressed from a downstream promoter, and is annotated on GeneID:100271849. [provided by RefSeq, Oct 2010].

mRNA and Protein(s)

mRNA	Protein	Name
NM_005919.4	NP_005910.1	myocyte-specific enhancer factor 2B isoform b
NM_005919.3	NP_005910.1	myocyte-specific enhancer factor 2B isoform b

Pathways from BioSystems
Gene Ontology
Bibliography

Related articles in PubMed

Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
Lauc G, Huffman JE, Pu?i? M, Zgaga L, Adamczyk B, Mu?ini? A, Novokmet M, Pola?ek O, Gornik O, Kri?ti? J, Keser T, Vitart V, Scheijen B, Uh HW, Molokhia M, Patrick AL, McKeigue P, Kol?i? I, Luki? IK, Swann O, van Leeuwen FN, Ruhaak LR, Houwing-Duistermaat JJ, Slagboom PE, Beekman M, de Craen AJ, Deelder AM, Zeng Q, Wang W, Hastie ND, Gyllensten U, Wilson JF, Wuhrer M, Wright AF, Rudd PM, Hayward C, Aulchenko Y, Campbell H, Rudan I
PLoS genetics9(1)e1003225(2013)

Expression of conjoined genes: another mechanism for gene regulation in eukaryotes.
Prakash T, Sharma VK, Adati N, Ozawa R, Kumar N, Nishida Y, Fujikake T, Takeda T, Taylor TD
PloS one5(10)e13284(2010 Oct)

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.
Yerges LM, Klei L, Cauley JA, Roeder K, Kammerer CM, Moffett SP, Ensrud KE, Nestlerode CS, Marshall LM, Hoffman AR, Lewis C, Lang TF, Barrett-Connor E, Ferrell RE, Orwoll ES, Zmuda JM,
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research24(12)2039-49(2009 Dec)

Regulatory role of MEF2D in serum induction of the c-jun promoter.
Han TH, Prywes R
Molecular and cellular biology15(6)2907-15(1995 Jun)

Human SRF-related proteins: DNA-binding properties and potential regulatory targets.
Pollock R, Treisman R
Genes & development5(12A)2327-41(1991 Dec)

GeneRIFs: Gene References Into Functions What's a GeneRIF?

Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
Title: Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.

Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
Title: Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.

Observational study of gene-disease association. (HuGE Navigator)
Title: High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.

Observational study of gene-disease association. (HuGE Navigator)
Title: Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

The following BORCS8-MEF2B gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the BORCS8-MEF2B cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1⁺/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.

***CloneID	Accession No.	Definition	**Vector	*Turnaround time	Price (USD)
OHu07743	NM_005919.4 Latest version!	Homo sapiens BORCS8-MEF2B readthrough (BORCS8-MEF2B), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$189.50-$265.30 $379.00
View Old Accession Versions >>
OHu07743	NM_005919.3	Homo sapiens BORCS8-MEF2B readthrough (BORCS8-MEF2B), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$189.50-$265.30 $379.00
Hide Old Accession Versions >>

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** GenScript guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories. In addition, please pay attention to the signal peptide, propeptide and transit peptide in target ORF, which may affect the choice of vector (N/C terminal tag vector).

***One clone ID might be correlated to multiple accession numbers, which share the same CDS sequence.

Reference Sequences (Refseq)

BORCS8-MEF2B ( NM_005919.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_005910.1 Homo sapiens BORCS8-MEF2B readthrough (BORCS8-MEF2B), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu07743
Clone ID Related Accession (Same CDS sequence)	NM_005919.4 , NM_005919.3
Accession Version	NM_005919.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1098bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-06-01
Organism	Homo sapiens(human)
Product	myocyte-specific enhancer factor 2B isoform b
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC002126.1 and X68502.1. On Jun 2, 2019 this sequence version replaced NM_005919.3. Transcript Variant: This variant (1) lacks two alternate exons in the 5' region and one alternate exon in the 3' region, compared to variant 2. This variant is thought to be protein coding because translation can reinitiate at the downstream AUG, resulting in expression of an isoform of MEF2B (geneID:100271849). Isoform b has a shorter and distinct C-terminus, compared to MEF2A isoform a (NP_001139257.1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: X68502.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## readthrough transcript :: includes exons from GeneID 729991, 100271849 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end.

ATGGGGAGGA AAAAAATCCA GATCTCCCGC ATCCTGGACC AAAGGAATCG GCAGGTGACG 
TTCACCAAGC GGAAGTTCGG GCTGATGAAG AAGGCCTATG AGCTGAGCGT GCTCTGTGAC 
TGTGAGATAG CCCTCATCAT CTTCAACAGC GCCAACCGCC TCTTCCAGTA TGCCAGCACG 
GACATGGACC GTGTGCTGCT GAAGTACACA GAGTACAGCG AGCCCCACGA GAGCCGCACC 
AACACTGACA TCCTCGAGAC GCTGAAGCGG AGGGGCATTG GCCTCGATGG GCCAGAGCTG 
GAGCCGGATG AAGGGCCTGA GGAGCCAGGA GAGAAGTTTC GGAGGCTGGC AGGCGAAGGG 
GGTGATCCGG CCTTGCCCCG ACCCCGGCTG TATCCTGCAG CTCCTGCTAT GCCCAGCCCA 
GATGTGGTAT ACGGGGCCTT ACCGCCACCA GGCTGTGACC CCAGTGGGCT TGGGGAAGCA 
CTGCCCGCCC AGAGCCGCCC ATCTCCCTTC CGACCAGCAG CCCCCAAAGC CGGGCCCCCA 
GGCCTGGTGC ACCCTCTCTT CTCACCAAGC CACCTCACCA GCAAGACACC ACCCCCACTG 
TACCTGCCGA CGGAAGGGCG GAGGTCAGAC CTGCCTGGTG GCCTGGCTGG GCCCCGAGGG 
GGACTAAACA CCTCCAGAAG CCTCTACAGT GGCCTGCAGA ACCCCTGCTC CACTGCAACT 
CCCGGACCCC CACTGGGGAG CTTCCCCTTC CTCCCCGGAG GCCCCCCAGT GGGGGCCGAA 
GCCTGGGCGA GGAGGGTCCC CCAACCCGCG GCGCCTCCCC GCCGACCCCC CCAGTCAGCA 
TCAAGTCTGA GCGCCTCTCT CCGGCCCCCG GGGGCCCCGG CGACTTTCCT AAGACCTTCC 
CCTATCCCTT GCTCCTCGCC CGGTCCCTGG CAGAGCCTCT GCGGCCTGGG CCCGCCCTGC 
GCCGGCTGCC CTTGGCCGAC GGCTGGCCCC GGTAGGAGAT CACCCGGTGG CACCAGCCCA 
GAGCGCTCGC CAGGTACGGC GAGGGCACGT GGGGACCCCA CCTCCCTCCA GGCCTCTTCA 
GAGAAGACCC AACAGTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_005910.1
CDS	289..1386
Translation	MGRKKIQISRILDQRNRQVTFTKRKFGLMKKAYELSVLCDCEIALIIFNSANRLFQYASTDMDRVLLKYTEYSEPHESRTNTDILETLKRRGIGLDGPELEPDEGPEEPGEKFRRLAGEGGDPALPRPRLYPAAPAMPSPDVVYGALPPPGCDPSGLGEALPAQSRPSPFRPAAPKAGPPGLVHPLFSPSHLTSKTPPPLYLPTEGRRSDLPGGLAGPRGGLNTSRSLYSGLQNPCSTATPGPPLGSFPFLPGGPPVGAEAWARRVPQPAAPPRRPPQSASSLSASLRPPGAPATFLRPSPIPCSSPGPWQSLCGLGPPCAGCPWPTAGPGRRSPGGTSPERSPGTARARGDPTSLQASSEKTQQ

Target ORF information:

RefSeq Version	NM_005919.4
Organism	Homo sapiens(human)
Definition	Homo sapiens BORCS8-MEF2B readthrough (BORCS8-MEF2B), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_005919.4

ORF Insert Sequence:

ATGGGGAGGA AAAAAATCCA GATCTCCCGC ATCCTGGACC AAAGGAATCG GCAGGTGACG 
TTCACCAAGC GGAAGTTCGG GCTGATGAAG AAGGCCTATG AGCTGAGCGT GCTCTGTGAC 
TGTGAGATAG CCCTCATCAT CTTCAACAGC GCCAACCGCC TCTTCCAGTA TGCCAGCACG 
GACATGGACC GTGTGCTGCT GAAGTACACA GAGTACAGCG AGCCCCACGA GAGCCGCACC 
AACACTGACA TCCTCGAGAC GCTGAAGCGG AGGGGCATTG GCCTCGATGG GCCAGAGCTG 
GAGCCGGATG AAGGGCCTGA GGAGCCAGGA GAGAAGTTTC GGAGGCTGGC AGGCGAAGGG 
GGTGATCCGG CCTTGCCCCG ACCCCGGCTG TATCCTGCAG CTCCTGCTAT GCCCAGCCCA 
GATGTGGTAT ACGGGGCCTT ACCGCCACCA GGCTGTGACC CCAGTGGGCT TGGGGAAGCA 
CTGCCCGCCC AGAGCCGCCC ATCTCCCTTC CGACCAGCAG CCCCCAAAGC CGGGCCCCCA 
GGCCTGGTGC ACCCTCTCTT CTCACCAAGC CACCTCACCA GCAAGACACC ACCCCCACTG 
TACCTGCCGA CGGAAGGGCG GAGGTCAGAC CTGCCTGGTG GCCTGGCTGG GCCCCGAGGG 
GGACTAAACA CCTCCAGAAG CCTCTACAGT GGCCTGCAGA ACCCCTGCTC CACTGCAACT 
CCCGGACCCC CACTGGGGAG CTTCCCCTTC CTCCCCGGAG GCCCCCCAGT GGGGGCCGAA 
GCCTGGGCGA GGAGGGTCCC CCAACCCGCG GCGCCTCCCC GCCGACCCCC CCAGTCAGCA 
TCAAGTCTGA GCGCCTCTCT CCGGCCCCCG GGGGCCCCGG CGACTTTCCT AAGACCTTCC 
CCTATCCCTT GCTCCTCGCC CGGTCCCTGG CAGAGCCTCT GCGGCCTGGG CCCGCCCTGC 
GCCGGCTGCC CTTGGCCGAC GGCTGGCCCC GGTAGGAGAT CACCCGGTGG CACCAGCCCA 
GAGCGCTCGC CAGGTACGGC GAGGGCACGT GGGGACCCCA CCTCCCTCCA GGCCTCTTCA 
GAGAAGACCC AACAGTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

BORCS8-MEF2B ( NM_005919.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_005910.1 Homo sapiens BORCS8-MEF2B readthrough (BORCS8-MEF2B), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu07743
Clone ID Related Accession (Same CDS sequence)	NM_005919.4 , NM_005919.3
Accession Version	NM_005919.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1098bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2018-11-23
Organism	Homo sapiens(human)
Product	myocyte-specific enhancer factor 2B isoform b
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC002126.1 and X68502.1. On or before Mar 11, 2009 this sequence version replaced NM_001134794.1, NM_005919.2. Transcript Variant: This variant (1) lacks two alternate exons in the 5' region and one alternate exon in the 3' region, compared to variant 2. This variant is thought to be protein coding because translation can reinitiate at the downstream AUG, resulting in expression of an isoform of MEF2B (geneID:100271849). Isoform b has a shorter and distinct C-terminus, compared to MEF2A isoform a (NP_001139257.1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: X68502.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## readthrough transcript :: includes exons from GeneID 729991, 100271849 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end.

ATGGGGAGGA AAAAAATCCA GATCTCCCGC ATCCTGGACC AAAGGAATCG GCAGGTGACG 
TTCACCAAGC GGAAGTTCGG GCTGATGAAG AAGGCCTATG AGCTGAGCGT GCTCTGTGAC 
TGTGAGATAG CCCTCATCAT CTTCAACAGC GCCAACCGCC TCTTCCAGTA TGCCAGCACG 
GACATGGACC GTGTGCTGCT GAAGTACACA GAGTACAGCG AGCCCCACGA GAGCCGCACC 
AACACTGACA TCCTCGAGAC GCTGAAGCGG AGGGGCATTG GCCTCGATGG GCCAGAGCTG 
GAGCCGGATG AAGGGCCTGA GGAGCCAGGA GAGAAGTTTC GGAGGCTGGC AGGCGAAGGG 
GGTGATCCGG CCTTGCCCCG ACCCCGGCTG TATCCTGCAG CTCCTGCTAT GCCCAGCCCA 
GATGTGGTAT ACGGGGCCTT ACCGCCACCA GGCTGTGACC CCAGTGGGCT TGGGGAAGCA 
CTGCCCGCCC AGAGCCGCCC ATCTCCCTTC CGACCAGCAG CCCCCAAAGC CGGGCCCCCA 
GGCCTGGTGC ACCCTCTCTT CTCACCAAGC CACCTCACCA GCAAGACACC ACCCCCACTG 
TACCTGCCGA CGGAAGGGCG GAGGTCAGAC CTGCCTGGTG GCCTGGCTGG GCCCCGAGGG 
GGACTAAACA CCTCCAGAAG CCTCTACAGT GGCCTGCAGA ACCCCTGCTC CACTGCAACT 
CCCGGACCCC CACTGGGGAG CTTCCCCTTC CTCCCCGGAG GCCCCCCAGT GGGGGCCGAA 
GCCTGGGCGA GGAGGGTCCC CCAACCCGCG GCGCCTCCCC GCCGACCCCC CCAGTCAGCA 
TCAAGTCTGA GCGCCTCTCT CCGGCCCCCG GGGGCCCCGG CGACTTTCCT AAGACCTTCC 
CCTATCCCTT GCTCCTCGCC CGGTCCCTGG CAGAGCCTCT GCGGCCTGGG CCCGCCCTGC 
GCCGGCTGCC CTTGGCCGAC GGCTGGCCCC GGTAGGAGAT CACCCGGTGG CACCAGCCCA 
GAGCGCTCGC CAGGTACGGC GAGGGCACGT GGGGACCCCA CCTCCCTCCA GGCCTCTTCA 
GAGAAGACCC AACAGTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_005910.1
CDS	728..1825
Translation	MGRKKIQISRILDQRNRQVTFTKRKFGLMKKAYELSVLCDCEIALIIFNSANRLFQYASTDMDRVLLKYTEYSEPHESRTNTDILETLKRRGIGLDGPELEPDEGPEEPGEKFRRLAGEGGDPALPRPRLYPAAPAMPSPDVVYGALPPPGCDPSGLGEALPAQSRPSPFRPAAPKAGPPGLVHPLFSPSHLTSKTPPPLYLPTEGRRSDLPGGLAGPRGGLNTSRSLYSGLQNPCSTATPGPPLGSFPFLPGGPPVGAEAWARRVPQPAAPPRRPPQSASSLSASLRPPGAPATFLRPSPIPCSSPGPWQSLCGLGPPCAGCPWPTAGPGRRSPGGTSPERSPGTARARGDPTSLQASSEKTQQ

Target ORF information:

RefSeq Version	NM_005919.3
Organism	Homo sapiens(human)
Definition	Homo sapiens BORCS8-MEF2B readthrough (BORCS8-MEF2B), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_005919.3

ORF Insert Sequence:

ATGGGGAGGA AAAAAATCCA GATCTCCCGC ATCCTGGACC AAAGGAATCG GCAGGTGACG 
TTCACCAAGC GGAAGTTCGG GCTGATGAAG AAGGCCTATG AGCTGAGCGT GCTCTGTGAC 
TGTGAGATAG CCCTCATCAT CTTCAACAGC GCCAACCGCC TCTTCCAGTA TGCCAGCACG 
GACATGGACC GTGTGCTGCT GAAGTACACA GAGTACAGCG AGCCCCACGA GAGCCGCACC 
AACACTGACA TCCTCGAGAC GCTGAAGCGG AGGGGCATTG GCCTCGATGG GCCAGAGCTG 
GAGCCGGATG AAGGGCCTGA GGAGCCAGGA GAGAAGTTTC GGAGGCTGGC AGGCGAAGGG 
GGTGATCCGG CCTTGCCCCG ACCCCGGCTG TATCCTGCAG CTCCTGCTAT GCCCAGCCCA 
GATGTGGTAT ACGGGGCCTT ACCGCCACCA GGCTGTGACC CCAGTGGGCT TGGGGAAGCA 
CTGCCCGCCC AGAGCCGCCC ATCTCCCTTC CGACCAGCAG CCCCCAAAGC CGGGCCCCCA 
GGCCTGGTGC ACCCTCTCTT CTCACCAAGC CACCTCACCA GCAAGACACC ACCCCCACTG 
TACCTGCCGA CGGAAGGGCG GAGGTCAGAC CTGCCTGGTG GCCTGGCTGG GCCCCGAGGG 
GGACTAAACA CCTCCAGAAG CCTCTACAGT GGCCTGCAGA ACCCCTGCTC CACTGCAACT 
CCCGGACCCC CACTGGGGAG CTTCCCCTTC CTCCCCGGAG GCCCCCCAGT GGGGGCCGAA 
GCCTGGGCGA GGAGGGTCCC CCAACCCGCG GCGCCTCCCC GCCGACCCCC CCAGTCAGCA 
TCAAGTCTGA GCGCCTCTCT CCGGCCCCCG GGGGCCCCGG CGACTTTCCT AAGACCTTCC 
CCTATCCCTT GCTCCTCGCC CGGTCCCTGG CAGAGCCTCT GCGGCCTGGG CCCGCCCTGC 
GCCGGCTGCC CTTGGCCGAC GGCTGGCCCC GGTAGGAGAT CACCCGGTGG CACCAGCCCA 
GAGCGCTCGC CAGGTACGGC GAGGGCACGT GGGGACCCCA CCTCCCTCCA GGCCTCTTCA 
GAGAAGACCC AACAGTGA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

PubMed

Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
PLoS genetics9(1)e1003225(2013)
Lauc G,Huffman JE,Pu?i? M,Zgaga L,Adamczyk B,Mu?ini? A,Novokmet M,Pola?ek O,Gornik O,Kri?ti? J,Keser T,Vitart V,Scheijen B,Uh HW,Molokhia M,Patrick AL,McKeigue P,Kol?i? I,Luki? IK,Swann O,van Leeuwen FN,Ruhaak LR,Houwing-Duistermaat JJ,Slagboom PE,Beekman M,de Craen AJ,Deelder AM,Zeng Q,Wang W,Hastie ND,Gyllensten U,Wilson JF,Wuhrer M,Wright AF,Rudd PM,Hayward C,Aulchenko Y,Campbell H,Rudan I

Expression of conjoined genes: another mechanism for gene regulation in eukaryotes.
PloS one5(10)e13284(2010 Oct)
Prakash T,Sharma VK,Adati N,Ozawa R,Kumar N,Nishida Y,Fujikake T,Takeda T,Taylor TD

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research24(12)2039-49(2009 Dec)
Yerges LM,Klei L,Cauley JA,Roeder K,Kammerer CM,Moffett SP,Ensrud KE,Nestlerode CS,Marshall LM,Hoffman AR,Lewis C,Lang TF,Barrett-Connor E,Ferrell RE,Orwoll ES,Zmuda JM,

Regulatory role of MEF2D in serum induction of the c-jun promoter.
Molecular and cellular biology15(6)2907-15(1995 Jun)
Han TH,Prywes R

Human SRF-related proteins: DNA-binding properties and potential regulatory targets.
Genes & development5(12A)2327-41(1991 Dec)
Pollock R,Treisman R

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BORCS8-MEF2B cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

Related articles in PubMed

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

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