AMMECR1 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	AMMECR1
Entrez Gene ID	9949
Full Name	Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
Synonyms	AMMERC1,MFHIEN
General protein information	Preferred Names Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 Names AMME syndrome candidate gene 1 protein Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: X Map Location: Xq23
Summary	The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2010].
Disorder MIM:	300195
Disorder Html:	Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, 300990 (3)

mRNA and Protein(s)

mRNA	Protein	Name
NM_001025580.1	NP_001020751.1	AMME syndrome candidate gene 1 protein isoform 2
NM_001025580.2	NP_001020751.1	AMME syndrome candidate gene 1 protein isoform 2
NM_015365.3	NP_056180.1	AMME syndrome candidate gene 1 protein isoform 1
NM_001171689.1	NP_001165160.1	AMME syndrome candidate gene 1 protein isoform 3
NM_001171689.2	NP_001165160.1	AMME syndrome candidate gene 1 protein isoform 3
NM_015365.2	NP_056180.1	AMME syndrome candidate gene 1 protein isoform 1

Pathways from BioSystems

Homologies

Homo sapiens (human)	AMMECR1	NP_056180.1
Drosophila melanogaster (fruit fly)	CG5902	NP_651201.1
Mus musculus (house mouse)	Ammecr1	NP_062369.1
Rattus norvegicus (Norway rat)	Ammecr1	XP_002730257.1
Danio rerio (zebrafish)	ammecr1	NP_956875.1
Oryza sativa (rice)	Os10g0573100	NP_001065469.1
Pan troglodytes (chimpanzee)	AMMECR1	XP_529104.2
	AMMECR1	XP_001099875.1
Anopheles gambiae (African malaria mosquito)	AgaP_AGAP000328	XP_310788.4
Caenorhabditis elegans (roundworm)	R166.3	NP_496270.1
Xenopus tropicalis (tropical clawed frog)	ammecr1	NP_001116966.1
Canis lupus familiaris (dog)	AMMECR1	XP_549183.3
Bos taurus (cattle)	AMMECR1	XP_003588186.2
Gallus gallus (chicken)	AMMECR1	XP_001234035.3
Arabidopsis thaliana (thale cress)	AT2G38710	NP_001031509.1

Gene Ontology
Bibliography

Related articles in PubMed

Inactivation of AMMECR1 is associated with growth, bone, and heart alterations.
Moys?s-Oliveira M, Giannuzzi G, Fish RJ, Rosenfeld JA, Petit F, Soares MF, Kulikowski LD, Di-Battista A, Zamariolli M, Xia F, Liehr T, Kosyakova N, Carvalheira G, Parker M, Seaby EG, Ennis S, Gilbert RD, Hagelstrom RT, Cremona ML, Li WL, Malhotra A, Chandrasekhar A, Perry DL, Taft RJ, McCarrier J, Basel DG, Andrieux J, Stumpp T, Antunes F, Pereira GJ, Neerman-Arbez M, Meloni VA, Drummond-Borg M, Melaragno MI, Reymond A
Human mutation39(2)281-291(2018 Feb)

Andreoletti G, Seaby EG, Dewing JM, O'Kelly I, Lachlan K, Gilbert RD, Ennis S
Journal of medical genetics54(4)269-277(2017 Apr)

X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.
Basel-Vanagaite L, Pillar N, Isakov O, Smirin-Yosef P, Lagovsky I, Orenstein N, Salmon-Divon M, Tamary H, Zaft T, Bazak L, Meyerovitch J, Pelli T, Botchan S, Farberov L, Weissglas-Volkov D, Shomron N
Gene60647-52(2017 Mar)

Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
Yang X, Coulombe-Huntington J, Kang S, Sheynkman GM, Hao T, Richardson A, Sun S, Yang F, Shen YA, Murray RR, Spirohn K, Begg BE, Duran-Frigola M, MacWilliams A, Pevzner SJ, Zhong Q, Trigg SA, Tam S, Ghamsari L, Sahni N, Yi S, Rodriguez MD, Balcha D, Tan G, Costanzo M, Andrews B, Boone C, Zhou XJ, Salehi-Ashtiani K, Charloteaux B, Chen AA, Calderwood MA, Aloy P, Roth FP, Hill DE, Iakoucheva LM, Xia Y, Vidal M
Cell164(4)805-17(2016 Feb)

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

We conclude that AMMECR1 is a critical gene in the pathogenesis of Alport syndrome with intellectual disability (Mental retardation), Midface hypoplasia and Elliptocytosis (AMME), causing midface hypoplasia and elliptocytosis and contributing to early speech and language delay, infantile hypotonia and hearing loss

Study provides further evidence that mutated AMMECR1 gene is responsible for this clinically recognizable X-linked condition, Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis (AMME complex) with variable expressivity.
Title: X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.

PH0010 from Pyrococcus horikoshii is highly homologous to human AMMECR 1C-terminal region
Title: Crystal structure of PH0010 from Pyrococcus horikoshii, which is highly homologous to human AMMECR 1C-terminal region.

The following AMMECR1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the AMMECR1 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)
OHu19188	NM_015365.3 Latest version!	Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$139.50-$195.30 $279.00
OHu30497	NM_001025580.2 Latest version!	Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$154.50-$216.30 $309.00
OHu04369	NM_001171689.2 Latest version!	Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$188.30 $269.00
View Old Accession Versions >>
OHu30497	NM_001025580.1	Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$154.50-$216.30 $309.00
OHu04369	NM_001171689.1	Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$188.30 $269.00
OHu19188	NM_015365.2	Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$139.50-$195.30 $279.00
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)

AMMECR1 ( NM_015365.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_056180.1 Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu19188
Clone ID Related Accession (Same CDS sequence)	NM_015365.3 , NM_015365.2
Accession Version	NM_015365.3 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1002bp) 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	2019-09-30
Organism	Homo sapiens(human)
Product	AMME syndrome candidate gene 1 protein isoform 1
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AJ007014.1, BC060813.1, BC037983.1 and BC051895.1. This sequence is a reference standard in the RefSeqGene project. On Nov 22, 2018 this sequence version replaced NM_015365.2. Transcript Variant: This variant (1) encodes the longest isoform (1). 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 :: SRR1660803.76746.1, SRR1660809.67929.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000262844.10/ ENSP00000262844.5 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTACCCACTG 
TTTGTAACAT GGAAGATTGG TCGAGACAAA AGATTACGTG GATGCATAGG TACTTTTTCT 
GCCATGAATT TGCATTCAGG ACTCAGGGAG TACACACTTA CCAGTGCCCT TAAAGATAGC 
CGTTTTCCCC CAATGACAAG GGATGAGCTG CCACGGCTTT TCTGCTCAGT GTCTCTGCTC 
ACTAACTTTG AAGATGTCTG TGATTATTTG GACTGGGAGG TGGGTGTACA TGGCATTAGA 
ATAGAATTCA TCAATGAAAA AGGATCAAAA CGCACCGCCA CCTACCTACC GGAGGTTGCA 
AAGGAGCAAG GATGGGACCA TATACAGACC ATAGACTCCT TATTGAGGAA AGGAGGATAC 
AAAGCTCCGA TTACTAATGA ATTCAGGAAA ACCATAAAAC TGACCAGGTA TCGTAGTGAA 
AAGATGACCC TGAGCTATGC TGAATACCTT GCTCATCGCC AGCATCATCA TTTCCAAAAT 
GGCATTGGGC ATCCCCTTCC GCCATACAAC CATTATTCCT GA

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

RefSeq	NP_056180.1
CDS	15..1016
Translation	MAAGCCGVKKQKLSSSPPSGSGGGGGASSSSHCSGESQCRAGELGLGGAGTRLNGLGGLTGGGSGSGCTLSPPQGCGGGGGGIALSPPPSCGVGTLLSTPAAATSSSPSSSSAASSSSPGSRKMVVSAEMCCFCFDVLYCHLYGYQQPRTPRFTNEPYPLFVTWKIGRDKRLRGCIGTFSAMNLHSGLREYTLTSALKDSRFPPMTRDELPRLFCSVSLLTNFEDVCDYLDWEVGVHGIRIEFINEKGSKRTATYLPEVAKEQGWDHIQTIDSLLRKGGYKAPITNEFRKTIKLTRYRSEKMTLSYAEYLAHRQHHHFQNGIGHPLPPYNHYS

Target ORF information:

RefSeq Version	NM_015365.3
Organism	Homo sapiens(human)
Definition	Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 1, mRNA.

Target ORF information:

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

NM_015365.3

ORF Insert Sequence:

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTACCCACTG 
TTTGTAACAT GGAAGATTGG TCGAGACAAA AGATTACGTG GATGCATAGG TACTTTTTCT 
GCCATGAATT TGCATTCAGG ACTCAGGGAG TACACACTTA CCAGTGCCCT TAAAGATAGC 
CGTTTTCCCC CAATGACAAG GGATGAGCTG CCACGGCTTT TCTGCTCAGT GTCTCTGCTC 
ACTAACTTTG AAGATGTCTG TGATTATTTG GACTGGGAGG TGGGTGTACA TGGCATTAGA 
ATAGAATTCA TCAATGAAAA AGGATCAAAA CGCACCGCCA CCTACCTACC GGAGGTTGCA 
AAGGAGCAAG GATGGGACCA TATACAGACC ATAGACTCCT TATTGAGGAA AGGAGGATAC 
AAAGCTCCGA TTACTAATGA ATTCAGGAAA ACCATAAAAC TGACCAGGTA TCGTAGTGAA 
AAGATGACCC TGAGCTATGC TGAATACCTT GCTCATCGCC AGCATCATCA TTTCCAAAAT 
GGCATTGGGC ATCCCCTTCC GCCATACAAC CATTATTCCT GA

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

AMMECR1 ( NM_015365.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_056180.1 Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu19188
Clone ID Related Accession (Same CDS sequence)	NM_015365.3 , NM_015365.2
Accession Version	NM_015365.2	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1002bp) 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	2017-12-26
Organism	Homo sapiens(human)
Product	AMME syndrome candidate gene 1 protein isoform 1
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AJ007014.1, BC060813.1, BC037983.1 and BC051895.1. This sequence is a reference standard in the RefSeqGene project. On Jul 19, 2005 this sequence version replaced NM_015365.1. Transcript Variant: This variant (1) encodes the longest isoform (1). ##Evidence-Data-START## Transcript exon combination :: SRR1660803.76746.1, SRR1803613.106568.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTACCCACTG 
TTTGTAACAT GGAAGATTGG TCGAGACAAA AGATTACGTG GATGCATAGG TACTTTTTCT 
GCCATGAATT TGCATTCAGG ACTCAGGGAG TACACACTTA CCAGTGCCCT TAAAGATAGC 
CGTTTTCCCC CAATGACAAG GGATGAGCTG CCACGGCTTT TCTGCTCAGT GTCTCTGCTC 
ACTAACTTTG AAGATGTCTG TGATTATTTG GACTGGGAGG TGGGTGTACA TGGCATTAGA 
ATAGAATTCA TCAATGAAAA AGGATCAAAA CGCACCGCCA CCTACCTACC GGAGGTTGCA 
AAGGAGCAAG GATGGGACCA TATACAGACC ATAGACTCCT TATTGAGGAA AGGAGGATAC 
AAAGCTCCGA TTACTAATGA ATTCAGGAAA ACCATAAAAC TGACCAGGTA TCGTAGTGAA 
AAGATGACCC TGAGCTATGC TGAATACCTT GCTCATCGCC AGCATCATCA TTTCCAAAAT 
GGCATTGGGC ATCCCCTTCC GCCATACAAC CATTATTCCT GA

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

RefSeq	NP_056180.1
CDS	82..1083
Translation	MAAGCCGVKKQKLSSSPPSGSGGGGGASSSSHCSGESQCRAGELGLGGAGTRLNGLGGLTGGGSGSGCTLSPPQGCGGGGGGIALSPPPSCGVGTLLSTPAAATSSSPSSSSAASSSSPGSRKMVVSAEMCCFCFDVLYCHLYGYQQPRTPRFTNEPYPLFVTWKIGRDKRLRGCIGTFSAMNLHSGLREYTLTSALKDSRFPPMTRDELPRLFCSVSLLTNFEDVCDYLDWEVGVHGIRIEFINEKGSKRTATYLPEVAKEQGWDHIQTIDSLLRKGGYKAPITNEFRKTIKLTRYRSEKMTLSYAEYLAHRQHHHFQNGIGHPLPPYNHYS

Target ORF information:

RefSeq Version	NM_015365.2
Organism	Homo sapiens(human)
Definition	Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 1, mRNA.

Target ORF information:

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

NM_015365.2

ORF Insert Sequence:

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTACCCACTG 
TTTGTAACAT GGAAGATTGG TCGAGACAAA AGATTACGTG GATGCATAGG TACTTTTTCT 
GCCATGAATT TGCATTCAGG ACTCAGGGAG TACACACTTA CCAGTGCCCT TAAAGATAGC 
CGTTTTCCCC CAATGACAAG GGATGAGCTG CCACGGCTTT TCTGCTCAGT GTCTCTGCTC 
ACTAACTTTG AAGATGTCTG TGATTATTTG GACTGGGAGG TGGGTGTACA TGGCATTAGA 
ATAGAATTCA TCAATGAAAA AGGATCAAAA CGCACCGCCA CCTACCTACC GGAGGTTGCA 
AAGGAGCAAG GATGGGACCA TATACAGACC ATAGACTCCT TATTGAGGAA AGGAGGATAC 
AAAGCTCCGA TTACTAATGA ATTCAGGAAA ACCATAAAAC TGACCAGGTA TCGTAGTGAA 
AAGATGACCC TGAGCTATGC TGAATACCTT GCTCATCGCC AGCATCATCA TTTCCAAAAT 
GGCATTGGGC ATCCCCTTCC GCCATACAAC CATTATTCCT GA

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

AMMECR1 ( NM_001025580.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001020751.1 Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu30497
Clone ID Related Accession (Same CDS sequence)	NM_001025580.1 , NM_001025580.2
Accession Version	NM_001025580.1	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 891bp) 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	2019-01-12
Organism	Homo sapiens(human)
Product	AMME syndrome candidate gene 1 protein isoform 2
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AJ007014.1, BC060813.1, BC037983.1 and BC051895.1. Transcript Variant: This variant (2) is missing an in-frame coding exon compared to variant 1, resulting in a shorter isoform (2) lacking an internal protein segment compared to isoform 1. ##Evidence-Data-START## Transcript exon combination :: BX648797.1, BC060813.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968968, SAMEA2142348 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTATGCCCTT 
AAAGATAGCC GTTTTCCCCC AATGACAAGG GATGAGCTGC CACGGCTTTT CTGCTCAGTG 
TCTCTGCTCA CTAACTTTGA AGATGTCTGT GATTATTTGG ACTGGGAGGT GGGTGTACAT 
GGCATTAGAA TAGAATTCAT CAATGAAAAA GGATCAAAAC GCACCGCCAC CTACCTACCG 
GAGGTTGCAA AGGAGCAAGG ATGGGACCAT ATACAGACCA TAGACTCCTT ATTGAGGAAA 
GGAGGATACA AAGCTCCGAT TACTAATGAA TTCAGGAAAA CCATAAAACT GACCAGGTAT 
CGTAGTGAAA AGATGACCCT GAGCTATGCT GAATACCTTG CTCATCGCCA GCATCATCAT 
TTCCAAAATG GCATTGGGCA TCCCCTTCCG CCATACAACC ATTATTCCTG A

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

RefSeq	NP_001020751.1
CDS	82..972
Translation	MAAGCCGVKKQKLSSSPPSGSGGGGGASSSSHCSGESQCRAGELGLGGAGTRLNGLGGLTGGGSGSGCTLSPPQGCGGGGGGIALSPPPSCGVGTLLSTPAAATSSSPSSSSAASSSSPGSRKMVVSAEMCCFCFDVLYCHLYGYQQPRTPRFTNEPYALKDSRFPPMTRDELPRLFCSVSLLTNFEDVCDYLDWEVGVHGIRIEFINEKGSKRTATYLPEVAKEQGWDHIQTIDSLLRKGGYKAPITNEFRKTIKLTRYRSEKMTLSYAEYLAHRQHHHFQNGIGHPLPPYNHYS

Target ORF information:

RefSeq Version	NM_001025580.1
Organism	Homo sapiens(human)
Definition	Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 2, mRNA.

Target ORF information:

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

NM_001025580.1

ORF Insert Sequence:

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTATGCCCTT 
AAAGATAGCC GTTTTCCCCC AATGACAAGG GATGAGCTGC CACGGCTTTT CTGCTCAGTG 
TCTCTGCTCA CTAACTTTGA AGATGTCTGT GATTATTTGG ACTGGGAGGT GGGTGTACAT 
GGCATTAGAA TAGAATTCAT CAATGAAAAA GGATCAAAAC GCACCGCCAC CTACCTACCG 
GAGGTTGCAA AGGAGCAAGG ATGGGACCAT ATACAGACCA TAGACTCCTT ATTGAGGAAA 
GGAGGATACA AAGCTCCGAT TACTAATGAA TTCAGGAAAA CCATAAAACT GACCAGGTAT 
CGTAGTGAAA AGATGACCCT GAGCTATGCT GAATACCTTG CTCATCGCCA GCATCATCAT 
TTCCAAAATG GCATTGGGCA TCCCCTTCCG CCATACAACC ATTATTCCTG A

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

AMMECR1 ( NM_001025580.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_001020751.1 Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu30497
Clone ID Related Accession (Same CDS sequence)	NM_001025580.1 , NM_001025580.2
Accession Version	NM_001025580.2 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 891bp) 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	2019-09-30
Organism	Homo sapiens(human)
Product	AMME syndrome candidate gene 1 protein isoform 2
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AJ007014.1, BC060813.1, BC037983.1 and BC051895.1. On May 31, 2019 this sequence version replaced NM_001025580.1. Transcript Variant: This variant (2) is missing an in-frame coding exon compared to variant 1, resulting in a shorter isoform (2) lacking an internal protein segment compared to isoform 1. 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 :: BC060813.1, SRR1660803.159998.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968968, SAMEA2142348 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTATGCCCTT 
AAAGATAGCC GTTTTCCCCC AATGACAAGG GATGAGCTGC CACGGCTTTT CTGCTCAGTG 
TCTCTGCTCA CTAACTTTGA AGATGTCTGT GATTATTTGG ACTGGGAGGT GGGTGTACAT 
GGCATTAGAA TAGAATTCAT CAATGAAAAA GGATCAAAAC GCACCGCCAC CTACCTACCG 
GAGGTTGCAA AGGAGCAAGG ATGGGACCAT ATACAGACCA TAGACTCCTT ATTGAGGAAA 
GGAGGATACA AAGCTCCGAT TACTAATGAA TTCAGGAAAA CCATAAAACT GACCAGGTAT 
CGTAGTGAAA AGATGACCCT GAGCTATGCT GAATACCTTG CTCATCGCCA GCATCATCAT 
TTCCAAAATG GCATTGGGCA TCCCCTTCCG CCATACAACC ATTATTCCTG A

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

RefSeq	NP_001020751.1
CDS	15..905
Translation	MAAGCCGVKKQKLSSSPPSGSGGGGGASSSSHCSGESQCRAGELGLGGAGTRLNGLGGLTGGGSGSGCTLSPPQGCGGGGGGIALSPPPSCGVGTLLSTPAAATSSSPSSSSAASSSSPGSRKMVVSAEMCCFCFDVLYCHLYGYQQPRTPRFTNEPYALKDSRFPPMTRDELPRLFCSVSLLTNFEDVCDYLDWEVGVHGIRIEFINEKGSKRTATYLPEVAKEQGWDHIQTIDSLLRKGGYKAPITNEFRKTIKLTRYRSEKMTLSYAEYLAHRQHHHFQNGIGHPLPPYNHYS

Target ORF information:

RefSeq Version	NM_001025580.2
Organism	Homo sapiens(human)
Definition	Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 2, mRNA.

Target ORF information:

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

NM_001025580.2

ORF Insert Sequence:

ATGGCGGCGG GTTGCTGCGG GGTGAAGAAG CAGAAACTGT CCAGTTCGCC CCCCTCTGGC 
TCGGGTGGCG GTGGTGGCGC CTCCTCCTCC TCCCACTGCA GCGGAGAGAG CCAGTGCCGA 
GCTGGGGAGC TGGGACTAGG AGGCGCCGGT ACGCGGCTCA ACGGGCTGGG AGGTCTAACC 
GGAGGAGGTA GCGGCAGCGG CTGTACCCTC TCTCCCCCCC AGGGCTGCGG CGGCGGCGGC 
GGGGGGATCG CCCTGTCGCC ACCTCCGAGC TGCGGAGTGG GGACCCTACT TTCTACCCCG 
GCCGCCGCCA CCTCTTCCTC ACCCTCCTCA TCGTCCGCCG CCTCGTCCTC ATCGCCGGGC 
TCCCGGAAGA TGGTGGTGTC AGCAGAGATG TGCTGCTTTT GCTTCGATGT GCTCTACTGT 
CACCTGTATG GATACCAGCA GCCCCGGACC CCCCGATTCA CCAACGAGCC CTATGCCCTT 
AAAGATAGCC GTTTTCCCCC AATGACAAGG GATGAGCTGC CACGGCTTTT CTGCTCAGTG 
TCTCTGCTCA CTAACTTTGA AGATGTCTGT GATTATTTGG ACTGGGAGGT GGGTGTACAT 
GGCATTAGAA TAGAATTCAT CAATGAAAAA GGATCAAAAC GCACCGCCAC CTACCTACCG 
GAGGTTGCAA AGGAGCAAGG ATGGGACCAT ATACAGACCA TAGACTCCTT ATTGAGGAAA 
GGAGGATACA AAGCTCCGAT TACTAATGAA TTCAGGAAAA CCATAAAACT GACCAGGTAT 
CGTAGTGAAA AGATGACCCT GAGCTATGCT GAATACCTTG CTCATCGCCA GCATCATCAT 
TTCCAAAATG GCATTGGGCA TCCCCTTCCG CCATACAACC ATTATTCCTG A

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

AMMECR1 ( NM_001171689.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001165160.1 Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 3, mRNA.

Price & Availability↑

CloneID	OHu04369
Clone ID Related Accession (Same CDS sequence)	NM_001171689.1 , NM_001171689.2
Accession Version	NM_001171689.1	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 633bp) 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	2019-01-12
Organism	Homo sapiens(human)
Product	AMME syndrome candidate gene 1 protein isoform 3
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA203031.1, AK091430.1, BC060813.1, BC037983.1 and BC051895.1. Transcript Variant: This variant (3) differs at the 5' end compared to variant 1, resulting in translation initiation from an in-frame downstream AUG, and a shorter isoform (3) compared to isoform 1. ##Evidence-Data-START## Transcript exon combination :: AK091430.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGTGGTGT CAGCAGAGAT GTGCTGCTTT TGCTTCGATG TGCTCTACTG TCACCTGTAT 
GGATACCAGC AGCCCCGGAC CCCCCGATTC ACCAACGAGC CCTACCCACT GTTTGTAACA 
TGGAAGATTG GTCGAGACAA AAGATTACGT GGATGCATAG GTACTTTTTC TGCCATGAAT 
TTGCATTCAG GACTCAGGGA GTACACACTT ACCAGTGCCC TTAAAGATAG CCGTTTTCCC 
CCAATGACAA GGGATGAGCT GCCACGGCTT TTCTGCTCAG TGTCTCTGCT CACTAACTTT 
GAAGATGTCT GTGATTATTT GGACTGGGAG GTGGGTGTAC ATGGCATTAG AATAGAATTC 
ATCAATGAAA AAGGATCAAA ACGCACCGCC ACCTACCTAC CGGAGGTTGC AAAGGAGCAA 
GGATGGGACC ATATACAGAC CATAGACTCC TTATTGAGGA AAGGAGGATA CAAAGCTCCG 
ATTACTAATG AATTCAGGAA AACCATAAAA CTGACCAGGT ATCGTAGTGA AAAGATGACC 
CTGAGCTATG CTGAATACCT TGCTCATCGC CAGCATCATC ATTTCCAAAA TGGCATTGGG 
CATCCCCTTC CGCCATACAA CCATTATTCC TGA

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

RefSeq	NP_001165160.1
CDS	638..1270
Translation	MVVSAEMCCFCFDVLYCHLYGYQQPRTPRFTNEPYPLFVTWKIGRDKRLRGCIGTFSAMNLHSGLREYTLTSALKDSRFPPMTRDELPRLFCSVSLLTNFEDVCDYLDWEVGVHGIRIEFINEKGSKRTATYLPEVAKEQGWDHIQTIDSLLRKGGYKAPITNEFRKTIKLTRYRSEKMTLSYAEYLAHRQHHHFQNGIGHPLPPYNHYS

Target ORF information:

RefSeq Version	NM_001171689.1
Organism	Homo sapiens(human)
Definition	Homo sapiens Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1), transcript variant 3, mRNA.

Target ORF information:

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

NM_001171689.1

ORF Insert Sequence:

ATGGTGGTGT CAGCAGAGAT GTGCTGCTTT TGCTTCGATG TGCTCTACTG TCACCTGTAT 
GGATACCAGC AGCCCCGGAC CCCCCGATTC ACCAACGAGC CCTACCCACT GTTTGTAACA 
TGGAAGATTG GTCGAGACAA AAGATTACGT GGATGCATAG GTACTTTTTC TGCCATGAAT 
TTGCATTCAG GACTCAGGGA GTACACACTT ACCAGTGCCC TTAAAGATAG CCGTTTTCCC 
CCAATGACAA GGGATGAGCT GCCACGGCTT TTCTGCTCAG TGTCTCTGCT CACTAACTTT 
GAAGATGTCT GTGATTATTT GGACTGGGAG GTGGGTGTAC ATGGCATTAG AATAGAATTC 
ATCAATGAAA AAGGATCAAA ACGCACCGCC ACCTACCTAC CGGAGGTTGC AAAGGAGCAA 
GGATGGGACC ATATACAGAC CATAGACTCC TTATTGAGGA AAGGAGGATA CAAAGCTCCG 
ATTACTAATG AATTCAGGAA AACCATAAAA CTGACCAGGT ATCGTAGTGA AAAGATGACC 
CTGAGCTATG CTGAATACCT TGCTCATCGC CAGCATCATC ATTTCCAAAA TGGCATTGGG 
CATCCCCTTC CGCCATACAA CCATTATTCC TGA

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

AMMECR1 ( NM_001171689.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_001165160.1 Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 3, mRNA.

Price & Availability↑

CloneID	OHu04369
Clone ID Related Accession (Same CDS sequence)	NM_001171689.1 , NM_001171689.2
Accession Version	NM_001171689.2 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 633bp) 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	2019-09-30
Organism	Homo sapiens(human)
Product	AMME syndrome candidate gene 1 protein isoform 3
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA203031.1, AK091430.1, BC060813.1, BC037983.1 and BC051895.1. On May 31, 2019 this sequence version replaced NM_001171689.1. Transcript Variant: This variant (3) differs at the 5' end compared to variant 1, resulting in translation initiation from an in-frame downstream AUG, and a shorter isoform (3) compared to isoform 1. 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 :: AK091430.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGTGGTGT CAGCAGAGAT GTGCTGCTTT TGCTTCGATG TGCTCTACTG TCACCTGTAT 
GGATACCAGC AGCCCCGGAC CCCCCGATTC ACCAACGAGC CCTACCCACT GTTTGTAACA 
TGGAAGATTG GTCGAGACAA AAGATTACGT GGATGCATAG GTACTTTTTC TGCCATGAAT 
TTGCATTCAG GACTCAGGGA GTACACACTT ACCAGTGCCC TTAAAGATAG CCGTTTTCCC 
CCAATGACAA GGGATGAGCT GCCACGGCTT TTCTGCTCAG TGTCTCTGCT CACTAACTTT 
GAAGATGTCT GTGATTATTT GGACTGGGAG GTGGGTGTAC ATGGCATTAG AATAGAATTC 
ATCAATGAAA AAGGATCAAA ACGCACCGCC ACCTACCTAC CGGAGGTTGC AAAGGAGCAA 
GGATGGGACC ATATACAGAC CATAGACTCC TTATTGAGGA AAGGAGGATA CAAAGCTCCG 
ATTACTAATG AATTCAGGAA AACCATAAAA CTGACCAGGT ATCGTAGTGA AAAGATGACC 
CTGAGCTATG CTGAATACCT TGCTCATCGC CAGCATCATC ATTTCCAAAA TGGCATTGGG 
CATCCCCTTC CGCCATACAA CCATTATTCC TGA

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

RefSeq	NP_001165160.1
CDS	638..1270
Translation	MVVSAEMCCFCFDVLYCHLYGYQQPRTPRFTNEPYPLFVTWKIGRDKRLRGCIGTFSAMNLHSGLREYTLTSALKDSRFPPMTRDELPRLFCSVSLLTNFEDVCDYLDWEVGVHGIRIEFINEKGSKRTATYLPEVAKEQGWDHIQTIDSLLRKGGYKAPITNEFRKTIKLTRYRSEKMTLSYAEYLAHRQHHHFQNGIGHPLPPYNHYS

Target ORF information:

RefSeq Version	NM_001171689.2
Organism	Homo sapiens(human)
Definition	Homo sapiens AMMECR nuclear protein 1 (AMMECR1), transcript variant 3, mRNA.

Target ORF information:

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

NM_001171689.2

ORF Insert Sequence:

ATGGTGGTGT CAGCAGAGAT GTGCTGCTTT TGCTTCGATG TGCTCTACTG TCACCTGTAT 
GGATACCAGC AGCCCCGGAC CCCCCGATTC ACCAACGAGC CCTACCCACT GTTTGTAACA 
TGGAAGATTG GTCGAGACAA AAGATTACGT GGATGCATAG GTACTTTTTC TGCCATGAAT 
TTGCATTCAG GACTCAGGGA GTACACACTT ACCAGTGCCC TTAAAGATAG CCGTTTTCCC 
CCAATGACAA GGGATGAGCT GCCACGGCTT TTCTGCTCAG TGTCTCTGCT CACTAACTTT 
GAAGATGTCT GTGATTATTT GGACTGGGAG GTGGGTGTAC ATGGCATTAG AATAGAATTC 
ATCAATGAAA AAGGATCAAA ACGCACCGCC ACCTACCTAC CGGAGGTTGC AAAGGAGCAA 
GGATGGGACC ATATACAGAC CATAGACTCC TTATTGAGGA AAGGAGGATA CAAAGCTCCG 
ATTACTAATG AATTCAGGAA AACCATAAAA CTGACCAGGT ATCGTAGTGA AAAGATGACC 
CTGAGCTATG CTGAATACCT TGCTCATCGC CAGCATCATC ATTTCCAAAA TGGCATTGGG 
CATCCCCTTC CGCCATACAA CCATTATTCC TGA

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

PubMed

Inactivation of AMMECR1 is associated with growth, bone, and heart alterations.
Human mutation39(2)281-291(2018 Feb)
Moys?s-Oliveira M,Giannuzzi G,Fish RJ,Rosenfeld JA,Petit F,Soares MF,Kulikowski LD,Di-Battista A,Zamariolli M,Xia F,Liehr T,Kosyakova N,Carvalheira G,Parker M,Seaby EG,Ennis S,Gilbert RD,Hagelstrom RT,Cremona ML,Li WL,Malhotra A,Chandrasekhar A,Perry DL,Taft RJ,McCarrier J,Basel DG,Andrieux J,Stumpp T,Antunes F,Pereira GJ,Neerman-Arbez M,Meloni VA,Drummond-Borg M,Melaragno MI,Reymond A

Journal of medical genetics54(4)269-277(2017 Apr)
Andreoletti G,Seaby EG,Dewing JM,O'Kelly I,Lachlan K,Gilbert RD,Ennis S

X-linked elliptocytosis with impaired growth is related to mutated AMMECR1.
Gene60647-52(2017 Mar)
Basel-Vanagaite L,Pillar N,Isakov O,Smirin-Yosef P,Lagovsky I,Orenstein N,Salmon-Divon M,Tamary H,Zaft T,Bazak L,Meyerovitch J,Pelli T,Botchan S,Farberov L,Weissglas-Volkov D,Shomron N

Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
Cell164(4)805-17(2016 Feb)
Yang X,Coulombe-Huntington J,Kang S,Sheynkman GM,Hao T,Richardson A,Sun S,Yang F,Shen YA,Murray RR,Spirohn K,Begg BE,Duran-Frigola M,MacWilliams A,Pevzner SJ,Zhong Q,Trigg SA,Tam S,Ghamsari L,Sahni N,Yi S,Rodriguez MD,Balcha D,Tan G,Costanzo M,Andrews B,Boone C,Zhou XJ,Salehi-Ashtiani K,Charloteaux B,Chen AA,Calderwood MA,Aloy P,Roth FP,Hill DE,Iakoucheva LM,Xia Y,Vidal M

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AMMECR1 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:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

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