HOXA2 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	HOXA2
Entrez Gene ID	3199
Full Name	homeobox A2
Synonyms	HOX1K,MCOHI
General protein information	Preferred Names homeobox A2 Names homeobox protein Hox-A2 homeobox protein Hox-1K
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 7 Map Location: 7p15.2
Summary	In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. The encoded protein may be involved in the placement of hindbrain segments in the proper location along the anterior-posterior axis during development. [provided by RefSeq, Jul 2008].
Disorder MIM:	604685
Disorder Html:	?Microtia, hearing impairment, and cleft palate (AR), 612290 (3); ?Microtia with or without hearing impairment (AD), 612290 (3)

mRNA and Protein(s)

mRNA	Protein	Name
NM_006735.3	NP_006726.1	homeobox protein Hox-A2
NM_006735.4	NP_006726.1	homeobox protein Hox-A2

Pathways from BioSystems

Homologies

Canis lupus familiaris (dog)	HOXA2	XP_851905.1
Bos taurus (cattle)	HOXA2	NP_001069322.1
Rattus norvegicus (Norway rat)	LOC100911443	XP_003752225.1
Gallus gallus (chicken)	HOXA2	NP_990481.1
Xenopus tropicalis (tropical clawed frog)	hoxa2	XP_004915456.1
Pan troglodytes (chimpanzee)	HOXA2	XP_527697.2
Mus musculus (house mouse)	Hoxa2	NP_034581.1
Homo sapiens (human)	HOXA2	NP_006726.1
	HOXA2	XP_001092920.1
Rattus norvegicus (Norway rat)	Hoxa2	NP_036713.2
Danio rerio (zebrafish)	hoxa2b	NP_571181.1

Gene Ontology
Bibliography

Related articles in PubMed

Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology.
Piceci F, Morlino S, Castori M, Buffone E, De Luca A, Grammatico P, Guida V
Clinical genetics91(5)774-779(2017 May)

Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia.
Hao S, Jin L, Li C, Wang H, Zheng F, Ma D, Zhang T
International journal of pediatric otorhinolaryngology9378-82(2017 Feb)

Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome.
Hao S, Jin L, Wang H, Li C, Zheng F, Ma D, Zhang T
The Journal of craniofacial surgery27(6)e583-6(2016 Sep)

Molecular Analysis of the HOXA2-Dependent Degradation of RCHY1.
Bridoux L, Deneyer N, Bergiers I, Rezsohazy R
PloS one10(10)e0141347(2015)

Aberrantly hypermethylated Homeobox A2 derepresses metalloproteinase-9 through TBP and promotes invasion in Nasopharyngeal carcinoma.
Li HP, Peng CC, Chung IC, Huang MY, Huang ST, Chen CC, Chang KP, Hsu CL, Chang YS
Oncotarget4(11)2154-65(2013 Nov)

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

The role of HOXA2 gene in dominant isolated microtia and the dysmorphogenetic effect of this gene on ear development
Title: Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology.

5 genomic variants in GSC, HOXA2 and PRKRA were identified through mutational analysis in Chinese patients with microtia.
Title: Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia.

The Hoxa2-mediated decay of RCHY1 involves both the 19S and 20S proteasome complexes
Title: Molecular Analysis of the HOXA2-Dependent Degradation of RCHY1.

HOXA2 acts as a suppressor or TBP-antagonist to inhibit MMP-9 expression; while methylation-mediated inactivation of HOXA2 in NPC derepresses MMP-9 production and increases invasion of NPC cells.
Title: Aberrantly hypermethylated Homeobox A2 derepresses metalloproteinase-9 through TBP and promotes invasion in Nasopharyngeal carcinoma.

we have identified a nonsense mutation (Q235*) in HOXA2 that segregates with bilateral nonsyndromic microtia and hearing loss through three generations of a family in an autosomal dominant pattern.
Title: HOXA2 haploinsufficiency in dominant bilateral microtia and hearing loss.

The following HOXA2 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the HOXA2 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.

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***CloneID	Accession No.	Definition	**Vector	*Turnaround time	Price (USD)
OHu19562	NM_006735.4 Latest version!	Homo sapiens homeobox A2 (HOXA2), 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 >>
OHu19562	NM_006735.3	Homo sapiens homeobox A2 (HOXA2), 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)

HOXA2 ( NM_006735.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_006726.1 Homo sapiens homeobox A2 (HOXA2), mRNA.

Price & Availability↑

CloneID	OHu19562
Clone ID Related Accession (Same CDS sequence)	NM_006735.3 , NM_006735.4
Accession Version	NM_006735.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1131bp) 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	2017-09-30
Organism	Homo sapiens(human)
Product	homeobox protein Hox-A2
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BF509655.1, AW292406.1, BE465040.1, AI581335.1 and AI796505.1. This sequence is a reference standard in the RefSeqGene project. On Oct 9, 2003 this sequence version replaced NM_006735.2. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BC130571.1, CN431833.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA2142670 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGAATTACG AATTTGAGCG AGAGATTGGT TTTATCAATA GCCAGCCGTC GCTCGCTGAG 
TGCCTGACAT CTTTTCCCCC TGTCGCTGAT ACATTTCAAA GTTCATCAAT CAAGACCTCG 
ACGCTTTCAC ACTCGACACT GATTCCTCCT CCTTTTGAGC AGACCATTCC CAGCCTGAAC 
CCCGGCAGTC ACCCTCGCCA CGGCGCTGGC GGCCGCCCCA AGCCGAGCCC CGCGGGCAGC 
CGCGGCAGCC CGGTGCCCGC CGGCGCCCTG CAGCCGCCCG AGTACCCCTG GATGAAGGAG 
AAGAAGGCGG CCAAGAAAAC CGCACTTCTG CCGGCCGCCG CCGCCGCCGC CACCGCCGCA 
GCCACCGGCC CTGCTTGCCT CAGCCACAAA GAATCCCTGG AAATCGCCGA TGGCAGCGGC 
GGGGGATCGC GGCGCCTGAG AACTGCTTAC ACCAACACAC AGCTTCTAGA GCTGGAAAAA 
GAATTTCATT TCAACAAGTA CCTTTGCAGA CCCCGAAGGG TGGAGATTGC AGCGCTGCTG 
GATTTGACTG AGAGACAAGT GAAAGTGTGG TTTCAGAACC GGAGGATGAA GCACAAGAGG 
CAGACCCAGT GCAAGGAAAA CCAAAACAGC GAAGGGAAAT GTAAAAGCCT TGAGGACTCC 
GAGAAAGTAG AGGAGGACGA GGAAGAGAAG ACGCTCTTTG AGCAAGCCCT TAGCGTCTCT 
GGGGCCCTTC TGGAGAGGGA AGGCTACACT TTTCAGCAAA ATGCCCTCTC TCAGCAGCAG 
GCTCCCAATG GACACAATGG CGACTCCCAA AGTTTCCCAG TCTCGCCTTT AACCAGCAAT 
GAGAAAAATC TGAAACATTT TCAGCACCAG TCACCCACTG TTCCCAACTG CTTGTCAACA 
ATGGGCCAGA ACTGTGGAGC TGGCCTAAAC AATGACAGTC CTGAGGCCCT TGAGGTCCCC 
TCTTTGCAGG ACTTTAGCGT TTTCTCCACA GATTCCTGCC TGCAGCTTTC AGATGCAGTT 
TCACCCAGTT TGCCAGGTTC CCTCGACAGT CCCGTAGATA TTTCAGCTGA CAGCTTAGAC 
TTTTTTACAG ACACACTCAC CACAATCGAC TTGCAGCATC TGAATTACTA A

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

RefSeq	NP_006726.1
CDS	276..1406
Translation	MNYEFEREIGFINSQPSLAECLTSFPPVADTFQSSSIKTSTLSHSTLIPPPFEQTIPSLNPGSHPRHGAGGRPKPSPAGSRGSPVPAGALQPPEYPWMKEKKAAKKTALLPAAAAAATAAATGPACLSHKESLEIADGSGGGSRRLRTAYTNTQLLELEKEFHFNKYLCRPRRVEIAALLDLTERQVKVWFQNRRMKHKRQTQCKENQNSEGKCKSLEDSEKVEEDEEEKTLFEQALSVSGALLEREGYTFQQNALSQQQAPNGHNGDSQSFPVSPLTSNEKNLKHFQHQSPTVPNCLSTMGQNCGAGLNNDSPEALEVPSLQDFSVFSTDSCLQLSDAVSPSLPGSLDSPVDISADSLDFFTDTLTTIDLQHLNY

Target ORF information:

RefSeq Version	NM_006735.3
Organism	Homo sapiens(human)
Definition	Homo sapiens homeobox A2 (HOXA2), mRNA.

Target ORF information:

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

NM_006735.3

ORF Insert Sequence:

ATGAATTACG AATTTGAGCG AGAGATTGGT TTTATCAATA GCCAGCCGTC GCTCGCTGAG 
TGCCTGACAT CTTTTCCCCC TGTCGCTGAT ACATTTCAAA GTTCATCAAT CAAGACCTCG 
ACGCTTTCAC ACTCGACACT GATTCCTCCT CCTTTTGAGC AGACCATTCC CAGCCTGAAC 
CCCGGCAGTC ACCCTCGCCA CGGCGCTGGC GGCCGCCCCA AGCCGAGCCC CGCGGGCAGC 
CGCGGCAGCC CGGTGCCCGC CGGCGCCCTG CAGCCGCCCG AGTACCCCTG GATGAAGGAG 
AAGAAGGCGG CCAAGAAAAC CGCACTTCTG CCGGCCGCCG CCGCCGCCGC CACCGCCGCA 
GCCACCGGCC CTGCTTGCCT CAGCCACAAA GAATCCCTGG AAATCGCCGA TGGCAGCGGC 
GGGGGATCGC GGCGCCTGAG AACTGCTTAC ACCAACACAC AGCTTCTAGA GCTGGAAAAA 
GAATTTCATT TCAACAAGTA CCTTTGCAGA CCCCGAAGGG TGGAGATTGC AGCGCTGCTG 
GATTTGACTG AGAGACAAGT GAAAGTGTGG TTTCAGAACC GGAGGATGAA GCACAAGAGG 
CAGACCCAGT GCAAGGAAAA CCAAAACAGC GAAGGGAAAT GTAAAAGCCT TGAGGACTCC 
GAGAAAGTAG AGGAGGACGA GGAAGAGAAG ACGCTCTTTG AGCAAGCCCT TAGCGTCTCT 
GGGGCCCTTC TGGAGAGGGA AGGCTACACT TTTCAGCAAA ATGCCCTCTC TCAGCAGCAG 
GCTCCCAATG GACACAATGG CGACTCCCAA AGTTTCCCAG TCTCGCCTTT AACCAGCAAT 
GAGAAAAATC TGAAACATTT TCAGCACCAG TCACCCACTG TTCCCAACTG CTTGTCAACA 
ATGGGCCAGA ACTGTGGAGC TGGCCTAAAC AATGACAGTC CTGAGGCCCT TGAGGTCCCC 
TCTTTGCAGG ACTTTAGCGT TTTCTCCACA GATTCCTGCC TGCAGCTTTC AGATGCAGTT 
TCACCCAGTT TGCCAGGTTC CCTCGACAGT CCCGTAGATA TTTCAGCTGA CAGCTTAGAC 
TTTTTTACAG ACACACTCAC CACAATCGAC TTGCAGCATC TGAATTACTA A

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

HOXA2 ( NM_006735.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_006726.1 Homo sapiens homeobox A2 (HOXA2), mRNA.

Price & Availability↑

CloneID	OHu19562
Clone ID Related Accession (Same CDS sequence)	NM_006735.3 , NM_006735.4
Accession Version	NM_006735.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1131bp) 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	2019-08-21
Organism	Homo sapiens(human)
Product	homeobox protein Hox-A2
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from BF509655.1, AW292406.1, BE465040.1, AI581335.1 and AI796505.1. This sequence is a reference standard in the RefSeqGene project. On Nov 23, 2018 this sequence version replaced NM_006735.3. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BC130571.1, CN431833.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA2142670 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000222718.7/ ENSP00000222718.5 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGAATTACG AATTTGAGCG AGAGATTGGT TTTATCAATA GCCAGCCGTC GCTCGCTGAG 
TGCCTGACAT CTTTTCCCCC TGTCGCTGAT ACATTTCAAA GTTCATCAAT CAAGACCTCG 
ACGCTTTCAC ACTCGACACT GATTCCTCCT CCTTTTGAGC AGACCATTCC CAGCCTGAAC 
CCCGGCAGTC ACCCTCGCCA CGGCGCTGGC GGCCGCCCCA AGCCGAGCCC CGCGGGCAGC 
CGCGGCAGCC CGGTGCCCGC CGGCGCCCTG CAGCCGCCCG AGTACCCCTG GATGAAGGAG 
AAGAAGGCGG CCAAGAAAAC CGCACTTCTG CCGGCCGCCG CCGCCGCCGC CACCGCCGCA 
GCCACCGGCC CTGCTTGCCT CAGCCACAAA GAATCCCTGG AAATCGCCGA TGGCAGCGGC 
GGGGGATCGC GGCGCCTGAG AACTGCTTAC ACCAACACAC AGCTTCTAGA GCTGGAAAAA 
GAATTTCATT TCAACAAGTA CCTTTGCAGA CCCCGAAGGG TGGAGATTGC AGCGCTGCTG 
GATTTGACTG AGAGACAAGT GAAAGTGTGG TTTCAGAACC GGAGGATGAA GCACAAGAGG 
CAGACCCAGT GCAAGGAAAA CCAAAACAGC GAAGGGAAAT GTAAAAGCCT TGAGGACTCC 
GAGAAAGTAG AGGAGGACGA GGAAGAGAAG ACGCTCTTTG AGCAAGCCCT TAGCGTCTCT 
GGGGCCCTTC TGGAGAGGGA AGGCTACACT TTTCAGCAAA ATGCCCTCTC TCAGCAGCAG 
GCTCCCAATG GACACAATGG CGACTCCCAA AGTTTCCCAG TCTCGCCTTT AACCAGCAAT 
GAGAAAAATC TGAAACATTT TCAGCACCAG TCACCCACTG TTCCCAACTG CTTGTCAACA 
ATGGGCCAGA ACTGTGGAGC TGGCCTAAAC AATGACAGTC CTGAGGCCCT TGAGGTCCCC 
TCTTTGCAGG ACTTTAGCGT TTTCTCCACA GATTCCTGCC TGCAGCTTTC AGATGCAGTT 
TCACCCAGTT TGCCAGGTTC CCTCGACAGT CCCGTAGATA TTTCAGCTGA CAGCTTAGAC 
TTTTTTACAG ACACACTCAC CACAATCGAC TTGCAGCATC TGAATTACTA A

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

RefSeq	NP_006726.1
CDS	184..1314
Translation	MNYEFEREIGFINSQPSLAECLTSFPPVADTFQSSSIKTSTLSHSTLIPPPFEQTIPSLNPGSHPRHGAGGRPKPSPAGSRGSPVPAGALQPPEYPWMKEKKAAKKTALLPAAAAAATAAATGPACLSHKESLEIADGSGGGSRRLRTAYTNTQLLELEKEFHFNKYLCRPRRVEIAALLDLTERQVKVWFQNRRMKHKRQTQCKENQNSEGKCKSLEDSEKVEEDEEEKTLFEQALSVSGALLEREGYTFQQNALSQQQAPNGHNGDSQSFPVSPLTSNEKNLKHFQHQSPTVPNCLSTMGQNCGAGLNNDSPEALEVPSLQDFSVFSTDSCLQLSDAVSPSLPGSLDSPVDISADSLDFFTDTLTTIDLQHLNY

Target ORF information:

RefSeq Version	NM_006735.4
Organism	Homo sapiens(human)
Definition	Homo sapiens homeobox A2 (HOXA2), mRNA.

Target ORF information:

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

NM_006735.4

ORF Insert Sequence:

ATGAATTACG AATTTGAGCG AGAGATTGGT TTTATCAATA GCCAGCCGTC GCTCGCTGAG 
TGCCTGACAT CTTTTCCCCC TGTCGCTGAT ACATTTCAAA GTTCATCAAT CAAGACCTCG 
ACGCTTTCAC ACTCGACACT GATTCCTCCT CCTTTTGAGC AGACCATTCC CAGCCTGAAC 
CCCGGCAGTC ACCCTCGCCA CGGCGCTGGC GGCCGCCCCA AGCCGAGCCC CGCGGGCAGC 
CGCGGCAGCC CGGTGCCCGC CGGCGCCCTG CAGCCGCCCG AGTACCCCTG GATGAAGGAG 
AAGAAGGCGG CCAAGAAAAC CGCACTTCTG CCGGCCGCCG CCGCCGCCGC CACCGCCGCA 
GCCACCGGCC CTGCTTGCCT CAGCCACAAA GAATCCCTGG AAATCGCCGA TGGCAGCGGC 
GGGGGATCGC GGCGCCTGAG AACTGCTTAC ACCAACACAC AGCTTCTAGA GCTGGAAAAA 
GAATTTCATT TCAACAAGTA CCTTTGCAGA CCCCGAAGGG TGGAGATTGC AGCGCTGCTG 
GATTTGACTG AGAGACAAGT GAAAGTGTGG TTTCAGAACC GGAGGATGAA GCACAAGAGG 
CAGACCCAGT GCAAGGAAAA CCAAAACAGC GAAGGGAAAT GTAAAAGCCT TGAGGACTCC 
GAGAAAGTAG AGGAGGACGA GGAAGAGAAG ACGCTCTTTG AGCAAGCCCT TAGCGTCTCT 
GGGGCCCTTC TGGAGAGGGA AGGCTACACT TTTCAGCAAA ATGCCCTCTC TCAGCAGCAG 
GCTCCCAATG GACACAATGG CGACTCCCAA AGTTTCCCAG TCTCGCCTTT AACCAGCAAT 
GAGAAAAATC TGAAACATTT TCAGCACCAG TCACCCACTG TTCCCAACTG CTTGTCAACA 
ATGGGCCAGA ACTGTGGAGC TGGCCTAAAC AATGACAGTC CTGAGGCCCT TGAGGTCCCC 
TCTTTGCAGG ACTTTAGCGT TTTCTCCACA GATTCCTGCC TGCAGCTTTC AGATGCAGTT 
TCACCCAGTT TGCCAGGTTC CCTCGACAGT CCCGTAGATA TTTCAGCTGA CAGCTTAGAC 
TTTTTTACAG ACACACTCAC CACAATCGAC TTGCAGCATC TGAATTACTA A

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

PubMed

Identification of a second HOXA2 nonsense mutation in a family with autosomal dominant non-syndromic microtia and distinctive ear morphology.
Clinical genetics91(5)774-779(2017 May)
Piceci F,Morlino S,Castori M,Buffone E,De Luca A,Grammatico P,Guida V

Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia.
International journal of pediatric otorhinolaryngology9378-82(2017 Feb)
Hao S,Jin L,Li C,Wang H,Zheng F,Ma D,Zhang T

Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome.
The Journal of craniofacial surgery27(6)e583-6(2016 Sep)
Hao S,Jin L,Wang H,Li C,Zheng F,Ma D,Zhang T

Molecular Analysis of the HOXA2-Dependent Degradation of RCHY1.
PloS one10(10)e0141347(2015)
Bridoux L,Deneyer N,Bergiers I,Rezsohazy R

Aberrantly hypermethylated Homeobox A2 derepresses metalloproteinase-9 through TBP and promotes invasion in Nasopharyngeal carcinoma.
Oncotarget4(11)2154-65(2013 Nov)
Li HP,Peng CC,Chung IC,Huang MY,Huang ST,Chen CC,Chang KP,Hsu CL,Chang YS

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HOXA2 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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