Gene Symbol | Hoxd13 |
Entrez Gene ID | 288154 |
Full Name | homeo box D13 |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
ORF » Species Summary » Rattus norvegicus » Hoxd13 cDNA ORF clone
Gene Symbol | Hoxd13 |
Entrez Gene ID | 288154 |
Full Name | homeo box D13 |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
mRNA | Protein | Name |
---|---|---|
NM_001105886.1 | NP_001099356.1 | homeobox protein Hox-D13 |
Homo sapiens (human) | HOXD13 | NP_000514.2 |
Gallus gallus (chicken) | HOXD13 | NP_990765.1 |
Pan troglodytes (chimpanzee) | HOXD13 | XP_525967.2 |
Bos taurus (cattle) | EVX2 | XP_003585777.2 |
Mus musculus (house mouse) | Hoxd13 | NP_032301.2 |
Xenopus tropicalis (tropical clawed frog) | hoxd13 | XP_002935723.1 |
LOC703825 | XP_001092153.2 | |
Rattus norvegicus (Norway rat) | Hoxd13 | NP_001099356.1 |
Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly.
Wang B, Li N, Geng J, Wang Z, Fu Q, Wang J, Xu Y
Congenital anomalies57(1)4-7(2017 Jan)
Evolution of Hoxa11 regulation in vertebrates is linked to the pentadactyl state.
Kherdjemil Y, Lalonde RL, Sheth R, Dumouchel A, de Martino G, Pineault KM, Wellik DM, Stadler HS, Akimenko MA, Kmita M
Nature539(7627)89-92(2016 11)
Maternal exposure to di-n-butyl phthalate (DBP) induces combined anorectal and urogenital malformations in male rat offspring.
Zhu YP, Li EH, Sun WL, Xu DL, Liu ZH, Zhao W, Wood K, Xia SJ, Jiang JT
Reproductive toxicology (Elmsford, N.Y.)61169-76(2016 06)
A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation.
Ibrahim DM, Tayebi N, Knaus A, Stiege AC, Sahebzamani A, Hecht J, Mundlos S, Spielmann M
American journal of medical genetics. Part A170(3)615-21(2016 Mar)
Molecular mechanism of Hoxd13-mediated congenital malformations in rat embryos.
Wang F, Du M, Wang R, Zhou J, Zhang W, Li H
International journal of clinical and experimental pathology8(12)15591-8(2015)
GeneRIFs: Gene References Into Functions What's a GeneRIF?
Hoxd13 expression was decreased in rat embryos with congenital malformations. The administration of exogenous Hoxd13 alleviated fetal malformation probably through stimulation of Slim1 expression and Wnt/beta-catenin signaling pathway.
Title: Molecular mechanism of Hoxd13-mediated congenital malformations in rat embryos.
The expression of Gli3, regulated by HOXD13, may play a role in idiopathic congenital talipes equinovarus.
Title: The expression of Gli3, regulated by HOXD13, may play a role in idiopathic congenital talipes equinovarus.
The following Hoxd13 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the Hoxd13 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 | ORa04379 | |
Clone ID Related Accession (Same CDS sequence) | NM_001105886.1 | |
Accession Version | NM_001105886.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 996bp) 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 | Rattus norvegicus(Norway rat) | |
Product | homeobox protein Hox-D13 | |
Comment | Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from CH473949.1. On or before Oct 3, 2007 this sequence version replaced XM_221511.3, XM_001063399.1. 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## RNAseq introns :: single sample supports all introns SAMEA2689604, SAMN01906348 [ECO:0000348] ##Evidence-Data-END## |
1 | ATGGATGGGC TGCGGGCGGA CGGCGGGGCC GCTGGGGCGG CACCGGCCTC CTCCTCCTCC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001099356.1 |
CDS | 24..1019 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001105886.1 |
1 | ATGGATGGGC TGCGGGCGGA CGGCGGGGCC GCTGGGGCGG CACCGGCCTC CTCCTCCTCC |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly. |
Evolution of Hoxa11 regulation in vertebrates is linked to the pentadactyl state. |
Maternal exposure to di-n-butyl phthalate (DBP) induces combined anorectal and urogenital malformations in male rat offspring. |
A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation. |
Molecular mechanism of Hoxd13-mediated congenital malformations in rat embryos. |