Utp6 cDNA ORF clone, Mus musculus(house mouse)
Gene Symbol | Utp6 |
Entrez Gene ID | 216987 |
Full Name | UTP6 small subunit processome component |
Synonyms | 4732497O03Rik,HCA66 |
General protein information |
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Gene Type | protein-coding |
Organism | Mus musculus(house mouse) |
Genome |
mRNA and Protein(s)
mRNA | Protein | Name |
---|---|---|
NM_144826.3 | NP_659075.1 | U3 small nucleolar RNA-associated protein 6 homolog |

Pan troglodytes (chimpanzee) | UTP6 | XP_511397.4 |
Danio rerio (zebrafish) | utp6 | NP_001104677.1 |
Arabidopsis thaliana (thale cress) | AT4G28200 | NP_194549.1 |
UTP6 | XP_001112332.1 | |
Canis lupus familiaris (dog) | UTP6 | XP_853877.1 |
Bos taurus (cattle) | UTP6 | NP_001092610.1 |
Anopheles gambiae (African malaria mosquito) | AgaP_AGAP008427 | XP_317018.3 |
Oryza sativa (rice) | Os02g0103900 | NP_001045609.1 |
Mus musculus (house mouse) | Utp6 | NP_659075.1 |
Gallus gallus (chicken) | UTP6 | NP_001006207.1 |
Drosophila melanogaster (fruit fly) | CG7246 | NP_572520.1 |
Homo sapiens (human) | UTP6 | NP_060898.2 |
Rattus norvegicus (Norway rat) | Utp6 | XP_006247026.1 |
Xenopus tropicalis (tropical clawed frog) | utp6 | NP_001016855.1 |

Related articles in PubMed
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome.
Venturin M, Carra S, Gaudenzi G, Brunelli S, Gallo GR, Moncini S, Cotelli F, Riva P
Journal of medical genetics51(7)436-43(2014 Jul)
A systems approach reveals that the myogenesis genome network is regulated by the transcriptional repressor RP58.
Yokoyama S, Ito Y, Ueno-Kudoh H, Shimizu H, Uchibe K, Albini S, Mitsuoka K, Miyaki S, Kiso M, Nagai A, Hikata T, Osada T, Fukuda N, Yamashita S, Harada D, Mezzano V, Kasai M, Puri PL, Hayashizaki Y, Okado H, Hashimoto M, Asahara H
Developmental cell17(6)836-48(2009 Dec)
Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients.
Piddubnyak V, Rigou P, Michel L, Rain JC, Geneste O, Wolkenstein P, Vidaud D, Hickman JA, Mauviel A, Poyet JL
Cell death and differentiation14(6)1222-33(2007 Jun)
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval.
Venturin M, Bentivegna A, Moroni R, Larizza L, Riva P
Annals of human genetics69(Pt 5)508-16(2005 Sep)
Bioinformatics and cellular signaling.
Papin J, Subramaniam S
Current opinion in biotechnology15(1)78-81(2004 Feb)
GeneRIFs: Gene References Into Functions What's a GeneRIF?
Results suggest that reduced expression of HCA66, owing to haploinsufficiency of HCA66 gene, could render NF1 microdeleted patients-derived cells less susceptible to apoptosis.
Title: Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients.
The following Utp6 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the Utp6 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 | OMu15129 | |
Clone ID Related Accession (Same CDS sequence) | NM_144826.3 | |
Accession Version | NM_144826.3 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 1794bp) Protein sequence SNP |
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Vector | pcDNA3.1+/C-(K)DYK or customized vector | ![]() |
Clone information | Clone Map | ![]() |
Tag on pcDNA3.1+/C-(K)DYK | C terminal DYKDDDDK tags | |
ORF Insert Method | CloneEZ™ Seamless cloning technology | |
Insert Structure | linear | |
Update Date | 2019-08-03 | |
Organism | Mus musculus(house mouse) | |
Product | U3 small nucleolar RNA-associated protein 6 homolog | |
Comment | Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from AK029151.1. On Apr 5, 2007 this sequence version replaced NM_144826.2. ##Evidence-Data-START## Transcript exon combination :: AK029151.1, SRR1660821.122685.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMN01164135, SAMN01164143 [ECO:0000348] ##Evidence-Data-END## |
1 | ATGGCGGAGA TAATTCAGGA ACGTATAGAA GATCGAATCC CGGAGTTGGA ACAGCTGGAG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_659075.1 |
CDS | 79..1872 |
Translation |

Target ORF information:
Target ORF information:
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ORF Insert Sequence:
1 | ATGGCGGAGA TAATTCAGGA ACGTATAGAA GATCGAATCC CGGAGTTGGA ACAGCTGGAG |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
![]() |
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome. |
![]() |
A systems approach reveals that the myogenesis genome network is regulated by the transcriptional repressor RP58. |
![]() |
Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients. |
![]() |
Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval. |
![]() |
Bioinformatics and cellular signaling. |