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Homeobox D13 Proteins (HOXD13)

HOXD13 belongs to the homeobox family of genes. Additionally we are shipping Homeobox D13 Antibodies (72) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
HOXD13 14654  
Rat HOXD13 HOXD13 288154  
HOXD13 3239 P35453
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Top Homeobox D13 Proteins at antibodies-online.com

Showing 5 out of 5 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Wheat germ Human GST tag 2 μg Log in to see 9 Days
$333.33
Details
Yeast Heterodontus francisci His tag   1 mg Log in to see 56 to 66 Days
$2,746.33
Details
Yeast Chicken His tag   1 mg Log in to see 56 to 66 Days
$2,799.50
Details

HOXD13 Proteins by Origin and Source

Origin Expressed in Conjugate
Mouse (Murine)

Human ,
,

More Proteins for Homeobox D13 (HOXD13) Interaction Partners

Zebrafish Homeobox D13 (HOXD13) interaction partners

  1. Data show that cis (show CISH Proteins)-regulatory elements driving Hoxd gene expression in distal limbs are present in fish.

Mouse (Murine) Homeobox D13 (HOXD13) interaction partners

  1. The age-associated accumulation of somatic mutations that occurs in the Nup98 (show NUP98 Proteins)-HOXD13 (NHD13) mouse model of leukemia progression was significantly elevated by co-expression of a PKR (show EIF2AK2 Proteins) transgene.

  2. Shox2 (show SHOX2 Proteins) expression restricted to the proximal limb along with Hoxd9 (show HOXD9 Proteins) and Hoxa11 (show HOXA11 Proteins) expression, juxtaposing the distal expression of Hoxa13 (show HOXA13 Proteins) and Hoxd13.

  3. Data indicate that loss of cyclin-dependent kinase inhibitor p15 (p15Ink4b (show CDKN2B Proteins)) collaborates with oncogene (show RAB1A Proteins) fusion protein Nup98 (show NUP98 Proteins)-HoxD13 transgene in the development of predominantly myeloid neoplasms.

  4. study elucidated the mechanism underlying a novel missense mutation in HOXD13 (Q317K) associated with a complex hand and foot malformation phenotype; results show that the mutation results in a shift in the binding profile of the mutant toward a bicoid/PITX1 (show PITX1 Proteins) motif

  5. providing synpolydactyly limb explant cultures with cells expressing either HOXD13 or WNT5A (show WNT5A Proteins) led to a non-cell autonomous partial rescue of cell polarity the perichondral region and restored the expression of perichondral markers.

  6. a slight and transient deregulation of Hoxd13 expression can readily affect the relative lengths of limb segments during development

  7. Mutation of a zinc-binding residue in the glycine receptor (show GLRB Proteins) alpha1 changes ethanol sensitivity in vitro and alcohol consumption in Glra1 (show GLRA1 Proteins)(D80A) knock-in mice.

  8. TM3 (show TPM1 Proteins)-4 loop subdomains are important for functional reconstitution of glycine receptors by independent domains

  9. findings show that expression of NUP98 (show NUP98 Proteins)-HOXD13 impairs class switch recombination and reduces the antibody-mediated immune response, in addition to its role in leukemia

  10. Mice expressing both the FLT3 (show FLT3 Proteins)/ITD and Nup98 (show NUP98 Proteins)-HoxD13 (NHD13) fusion gene developed acute myeloid leukemia (show BCL11A Proteins) with 100% penetrance

Human Homeobox D13 (HOXD13) interaction partners

  1. HOXD13 methylation is a common event in primary breast cancer and is associated with poor survival of breast cancer patients.

  2. A 27 bp expansion mutation in exon 1 of HOXD13 was associated with autosomal dominant synpolydactyly in a Chinese family.

  3. Linkage analysis of the syndactyly type 1 subtype c (SD1-c) phenotype based on two Chinese families with 3/4 fingers syndactyly shows that two missense mutations in codon 306 of HOXD13 underlie SD1-c.

  4. Identification of a novel c.659G>C (p.Gly220Ala) mutation outside the HOXD13 homeodomain responsible for synpolydactyly in a Chinese family.

  5. A genome-wide array-comparative genomic hybridization (aCGH) analysis revealed global chromosomal aberration in MWCNTs-treated clones, predominantly at chromosome 2q31-32, where the potential oncogenes HOXD9 (show HOXD9 Proteins) and HOXD13 are located

  6. Data indicate increased levels of reactive oxygen species (ROS (show ROS1 Proteins)) were detected in bone marrow nucleated cells (BMNC) that express CD71 (show TFRC Proteins) in in NUP98 (show NUP98 Proteins)-HOXD13 (NHD13) transgenic mice, a murine model for myelodysplastic syndromes (MDS (show PAFAH1B1 Proteins)).

  7. Molecular characteristics of a HOXD13 synpolydactyly 1 nonsense mutation in a Chinese family.

  8. findings show that expression of NUP98 (show NUP98 Proteins)-HOXD13 impairs class switch recombination and reduces the antibody-mediated immune response, in addition to its role in leukemia

  9. Misexpression of HOXD13(G11A) in the developing chick limb phenocopied the human SPD phenotype

  10. This finding expands the phenotypic spectrum associated with HOXD13 mutations and advances our understanding of human limb development.

Homeobox D13 (HOXD13) Protein Profile

Protein Summary

This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly.

Gene names and symbols associated with Homeobox D13 Proteins (HOXD13)

  • homeobox D13 (HOXD13)
  • homeobox D13 (hoxd13)
  • homeobox D13 (LOC100218824)
  • homeo box D13a (hoxd13a)
  • glycine receptor, alpha 1 subunit (Glra1)
  • homeo box D13 (Hoxd13)
  • homeobox D13 (Hoxd13)
  • surfactant protein D (Sftpd)
  • B230397M16Rik protein
  • BDE protein
  • BDSD protein
  • Hox-4.8 protein
  • HOX4I protein
  • hoxd-13 protein
  • hoxd13 protein
  • nmf11 protein
  • oscillator protein
  • ot protein
  • SP-D protein
  • spasmodic protein
  • SPD protein
  • spdh protein
  • XHoxd13 protein
  • zgc:110511 protein

Protein level used designations for Homeobox D13 Proteins (HOXD13)

homeobox D13 , homeobox gene D-13 , glycine receptor 48 kDa subunit , glycine receptor strychnine-binding subunit , glycine receptor subunit alpha-1 , homeobox protein Hox-D13 , homeo box 4I , homeo box D13 , homeobox protein Hox-4I , homeobox protein Hox-4.8 , chox-4.8 , chox-4G , homeobox protein Hox-4G , homeobox protein hoxd13 , CP4 , PSP-D , lung surfactant protein D , pulmonary surfactant protein D , pulmonary surfactant-associated protein D , surfactant associated protein D , surfactant, pulmonary-associated protein D

GENE ID SPECIES
100301549 Oryctolagus cuniculus
399207 Xenopus laevis
470586 Pan troglodytes
100218824 Taeniopygia guttata
100271866 Felis catus
30407 Danio rerio
14654 Mus musculus
288154 Rattus norvegicus
3239 Homo sapiens
520424 Bos taurus
15433 Mus musculus
396415 Gallus gallus
100152793 Sus scrofa
25350 Rattus norvegicus
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