Gene Symbol | GOLGA7 |
Entrez Gene ID | 51125 |
Full Name | golgin A7 |
Synonyms | GCP16,GOLGA3AP1,GOLGA7A,HSPC041 |
General protein information |
|
Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Disorder MIM: |
ORF » Species Summary » Homo sapiens » GOLGA7 cDNA ORF clone
Gene Symbol | GOLGA7 |
Entrez Gene ID | 51125 |
Full Name | golgin A7 |
Synonyms | GCP16,GOLGA3AP1,GOLGA7A,HSPC041 |
General protein information |
|
Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Disorder MIM: |
mRNA | Protein | Name |
---|---|---|
NM_001002296.1 | NP_001002296.1 | golgin subfamily A member 7 isoform a |
NM_001362979.1 | NP_001349908.1 | golgin subfamily A member 7 isoform a |
NM_001002296.2 | NP_001002296.1 | golgin subfamily A member 7 isoform a |
NM_001174124.1 | NP_001167595.1 | golgin subfamily A member 7 isoform b |
NM_001362980.1 | NP_001349909.1 | golgin subfamily A member 7 isoform a |
NM_016099.2 | NP_057183.2 | golgin subfamily A member 7 isoform a |
Homo sapiens (human) | GOLGA7 | NP_001002296.1 |
Pan troglodytes (chimpanzee) | GOLGA7 | XP_519727.3 |
Canis lupus familiaris (dog) | GOLGA7 | XP_003432157.1 |
Mus musculus (house mouse) | Golga7 | NP_001035949.1 |
Gallus gallus (chicken) | GOLGA7 | NP_001006570.1 |
Danio rerio (zebrafish) | golga7 | NP_001099069.1 |
GOLGA7 | XP_001098475.2 | |
Bos taurus (cattle) | GOLGA7 | NP_001030561.1 |
Rattus norvegicus (Norway rat) | Golga7 | NP_001007732.1 |
Xenopus tropicalis (tropical clawed frog) | golga7 | NP_001016450.1 |
Caenorhabditis elegans (roundworm) | CELE_Y57G11C.33 | NP_001255818.1 |
Widespread macromolecular interaction perturbations in human genetic disorders.
Sahni N, Yi S, Taipale M, Fuxman Bass JI, Coulombe-Huntington J, Yang F, Peng J, Weile J, Karras GI, Wang Y, Kov?cs IA, Kamburov A, Krykbaeva I, Lam MH, Tucker G, Khurana V, Sharma A, Liu YY, Yachie N, Zhong Q, Shen Y, Palagi A, San-Miguel A, Fan C, Balcha D, Dricot A, Jordan DM, Walsh JM, Shah AA, Yang X, Stoyanova AK, Leighton A, Calderwood MA, Jacob Y, Cusick ME, Salehi-Ashtiani K, Whitesell LJ, Sunyaev S, Berger B, Barab?si AL, Charloteaux B, Hill DE, Hao T, Roth FP, Xia Y, Walhout AJM, Lindquist S, Vidal M
Cell161(3)647-660(2015 Apr)
MHC class II-associated proteins in B-cell exosomes and potential functional implications for exosome biogenesis.
Buschow SI, van Balkom BW, Aalberts M, Heck AJ, Wauben M, Stoorvogel W
Immunology and cell biology88(8)851-6(2010 Nov-Dec)
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S,
Diabetes care33(10)2250-3(2010 Oct)
Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD, , ,
American journal of human genetics85(5)628-42(2009 Nov)
Large-scale proteomics and phosphoproteomics of urinary exosomes.
Gonzales PA, Pisitkun T, Hoffert JD, Tchapyjnikov D, Star RA, Kleta R, Wang NS, Knepper MA
Journal of the American Society of Nephrology : JASN20(2)363-79(2009 Feb)
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.
Observational study of gene-disease association. (HuGE Navigator)
Title: Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
Data show that H- and N-Ras are palmitoylated by a human protein palmitoyltransferase encoded by the ZDHHC9 and GCP16 genes.
Title: DHHC9 and GCP16 constitute a human protein fatty acyltransferase with specificity for H- and N-Ras.
results indicate that GCP16 is the acylated membrane protein, associated with GCP170, and possibly involved in vesicular transport from the Golgi to the cell surface
Title: Identification and characterization of GCP16, a novel acylated Golgi protein that interacts with GCP170.
The following GOLGA7 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the GOLGA7 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 | OHu02130 | |
Clone ID Related Accession (Same CDS sequence) | NM_001002296.1 , NM_001362979.1 , NM_001002296.2 , NM_001362980.1 , NM_016099.2 | |
Accession Version | NM_001002296.1 | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 414bp) 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 | 2018-06-22 | |
Organism | Homo sapiens(human) | |
Product | golgin subfamily A member 7 isoform a | |
Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BC012032.1, BC001227.2, AF068291.1, AV650886.1, AF125102.1 and BG939345.1. Transcript Variant: This variant (2) represents the longest transcript and encodes the longer isoform (a). Variants 1, 2, 4 and 5 encode the same isoform (a). ##Evidence-Data-START## Transcript exon combination :: SRR1163657.254360.1, SRR1660805.38423.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001002296.1 |
CDS | 202..615 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001002296.1 |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
CloneID | OHu02130 | |
Clone ID Related Accession (Same CDS sequence) | NM_001002296.1 , NM_001362979.1 , NM_001002296.2 , NM_001362980.1 , NM_016099.2 | |
Accession Version | NM_001362979.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 414bp) 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 | 2018-06-14 | |
Organism | Homo sapiens(human) | |
Product | golgin subfamily A member 7 isoform a | |
Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BI546026.1, BC001227.2, AF068291.1, AV650886.1, AF125102.1 and BG939345.1. On May 4, 2018 this sequence version replaced XM_024447174.1. ##Evidence-Data-START## Transcript exon combination :: SRR1803614.22583.1, SRR1660807.220545.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001349908.1 |
CDS | 194..607 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001362979.1 |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
CloneID | OHu02130 | |
Clone ID Related Accession (Same CDS sequence) | NM_001002296.1 , NM_001362979.1 , NM_001002296.2 , NM_001362980.1 , NM_016099.2 | |
Accession Version | NM_001002296.2 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 414bp) 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 | 2019-10-24 | |
Organism | Homo sapiens(human) | |
Product | golgin subfamily A member 7 isoform a | |
Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC009630.14, BC012032.1, BC001227.2, AF068291.1, AV650886.1, AF125102.1 and BG939345.1. On May 17, 2019 this sequence version replaced NM_001002296.1. Transcript Variant: This variant (2) represents the longest transcript and encodes the longer isoform (a). Variants 1, 2, 4 and 5 encode the same isoform (a). ##Evidence-Data-START## Transcript exon combination :: SRR3476690.1134319.1, SRR3476690.394859.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000357743.9/ ENSP00000350378.4 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001002296.1 |
CDS | 274..687 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001002296.2 |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
CloneID | OHu02130 | |
Clone ID Related Accession (Same CDS sequence) | NM_001002296.1 , NM_001362979.1 , NM_001002296.2 , NM_001362980.1 , NM_016099.2 | |
Accession Version | NM_001362980.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 414bp) 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 | 2018-06-14 | |
Organism | Homo sapiens(human) | |
Product | golgin subfamily A member 7 isoform a | |
Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BP341683.1, HY131836.1, BC001227.2, AF068291.1, AV650886.1, AF125102.1 and BG939345.1. On May 4, 2018 this sequence version replaced XM_024447175.1. ##Evidence-Data-START## Transcript exon combination :: SRR1803613.178899.1, SRR1660803.81973.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA1968968 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001349909.1 |
CDS | 101..514 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001362980.1 |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
CloneID | OHu02130 | |
Clone ID Related Accession (Same CDS sequence) | NM_001002296.1 , NM_001362979.1 , NM_001002296.2 , NM_001362980.1 , NM_016099.2 | |
Accession Version | NM_016099.2 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 414bp) 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 | 2018-06-22 | |
Organism | Homo sapiens(human) | |
Product | golgin subfamily A member 7 isoform a | |
Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AL695304.1, BI553491.1, BC012032.1, BC001227.2, AF068291.1, AV650886.1, AF125102.1 and BG939345.1. On Jul 23, 2004 this sequence version replaced NM_016099.1. Transcript Variant: This variant (1) differs in the 5' UTR, compared to variant 2, and encodes the longer isoform (a). Variants 1, 2, 4 and 5 encode the same isoform (a). ##Evidence-Data-START## Transcript exon combination :: AB104615.1, SRR1803613.165732.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_057183.2 |
CDS | 79..492 |
Translation |
Target ORF information:
Target ORF information:
|
NM_016099.2 |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
CloneID | OHu12541 | |
Clone ID Related Accession (Same CDS sequence) | NM_001174124.1 | |
Accession Version | NM_001174124.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 405bp) 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 | 2019-12-27 | |
Organism | Homo sapiens(human) | |
Product | golgin subfamily A member 7 isoform b | |
Comment | Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AL695304.1, AK026613.1, AC009630.14 and BC001227.2. Transcript Variant: This variant (3) differs in the 5' UTR and uses an alternate splice site in the 3' coding region that results in a frameshift, compared to variant 2. The resulting isoform (b) has a shorter and distinct C-terminus, compared to isoform a. ##Evidence-Data-START## Transcript exon combination :: AK026613.1, SRR1163657.12841.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end. |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001167595.1 |
CDS | 79..483 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001174124.1 |
1 | ATGAGGCCGC AGCAGGCGCC GGTGTCCGGA AAGGTGTTCA TTCAGCGAGA CTACAGCAGT |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
Widespread macromolecular interaction perturbations in human genetic disorders. |
MHC class II-associated proteins in B-cell exosomes and potential functional implications for exosome biogenesis. |
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. |
Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. |
Large-scale proteomics and phosphoproteomics of urinary exosomes. |