The following NCAN gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the NCAN 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 | OHu20939 | |
| Clone ID Related Accession (Same CDS sequence) | NM_004386.3 , NM_004386.2 | |
| Accession Version | NM_004386.3 Latest version! | Documents for ORF clone product in default vector |
| Sequence Information | ORF Nucleotide Sequence (Length: 3966bp) 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 | 2019-12-30 | |
| Organism | Homo sapiens(human) | |
| Product | neurocan core protein precursor | |
| Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC003110.1, CN282070.1, AB210004.1 and AC138430.2. On Nov 22, 2018 this sequence version replaced NM_004386.2. 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 :: AB210004.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2145743, SAMEA2148874 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000252575.11/ ENSP00000252575.4 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: full length. | |
1 | ATGGGGGCCC CGTTTGTCTG GGCCTTGGGC CTTTTGATGC TGCAGATGCT GCTCTTTGTG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
| RefSeq | NP_004377.2 |
| CDS | 115..4080 |
| Translation |
Target ORF information:
Target ORF information:
|
 NM_004386.3 |
1 | ATGGGGGCCC CGTTTGTCTG GGCCTTGGGC CTTTTGATGC TGCAGATGCT GCTCTTTGTG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
| CloneID | OHu20939 | |
| Clone ID Related Accession (Same CDS sequence) | NM_004386.3 , NM_004386.2 | |
| Accession Version | NM_004386.2 | Documents for ORF clone product in default vector |
| Sequence Information | ORF Nucleotide Sequence (Length: 3966bp) 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 | 2017-10-01 | |
| Organism | Homo sapiens(human) | |
| Product | neurocan core protein precursor | |
| Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from CN282070.1, AB210004.1 and AC138430.2. On Dec 2, 2006 this sequence version replaced NM_004386.1. 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 :: AB210004.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2145743, SAMEA2148874 [ECO:0000348] ##Evidence-Data-END## | |
1 | ATGGGGGCCC CGTTTGTCTG GGCCTTGGGC CTTTTGATGC TGCAGATGCT GCTCTTTGTG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
| RefSeq | NP_004377.2 |
| CDS | 100..4065 |
| Translation |
Target ORF information:
Target ORF information:
|
NM_004386.2 |
1 | ATGGGGGCCC CGTTTGTCTG GGCCTTGGGC CTTTTGATGC TGCAGATGCT GCTCTTTGTG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study. |
Replication analysis of genetic association of the NCAN-CILP2 region with plasma lipid levels and non-alcoholic fatty liver disease in Asian and Pacific ethnic groups. |
NCAN Cross-Disorder Risk Variant Is Associated With Limbic Gray Matter Deficits in Healthy Subjects and Major Depression. |
A genome-wide supported psychiatric risk variant in NCAN influences brain function and cognitive performance in healthy subjects. |
Biological insights from 108 schizophrenia-associated genetic loci. |
