ORF » Species Summary » Homo sapiens » AMMECR1 cDNA ORF clone

AMMECR1 cDNA ORF clone, Homo sapiens(human)

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.

Online Only Promotion

Up to 50% OFF! Starting
from $49/clone
***CloneID Accession No. Definition **Vector *Turnaround time Price (USD) Select
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 9-11 $139.30
$199.00
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 5+ $230.30
$329.00
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 5+ $216.30
$309.00
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 5+ $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 9-11 $139.30
$199.00
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 5+ $230.30
$329.00
Hide Old Accession Versions >>

ORF Online Only Promotion

Next-day Shipping ORF Clones ( in default vector with tag)
1 Clone 30% OFF
2-4 Clone 40% OFF
5 or more Clone 50% OFF
All Other ORF Clones
30% OFF

*Business Day

** You may select a custom vector to replace pcDNA3.1+/C-(K)DYK after clone is added to cart.

** 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_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 1547222400000
    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. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    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
    CDS638..1270
    Translation

    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 AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_001171689.1

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    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 1569772800000
    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. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    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
    CDS638..1270
    Translation

    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 AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_001171689.2

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    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_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 1569772800000
    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. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    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
    CDS15..1016
    Translation

    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 AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_015365.3

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    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 1514217600000
    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. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    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
    CDS82..1083
    Translation

    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 AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_015365.2

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    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 1547222400000
    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. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    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
    CDS82..972
    Translation

    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 AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_001025580.1

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    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 1569772800000
    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. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    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
    CDS15..905
    Translation

    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 AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_001025580.2

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    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.

  • PubMed


    Anticancer research39(9)4637-4642(2019 Sep)
    Ge H,Cheng N,Xu X,Yang Z,Hoffman RM,Zhu J


    Inactivation of AMMECR1 is associated with growth, bone, and heart alterations.
    Human mutation39(2)281-291(2018 02)
    Moysés-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 04)
    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


REQUEST A QUOTE

EMAIL

gene@genscript.com

PHONE

1-877-436-7274

ONLINE FORM

Online Quote Submission

ONLINE FORM

Online Quote Submission