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Dymeclin Proteins (DYM)

DYM encodes a protein which is necessary for normal skeletal development and brain function. Additionally we are shipping Dymeclin Antibodies (35) and Dymeclin Kits (3) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
DYM 54808 Q7RTS9
DYM 69190 Q8CHY3
DYM 291433  
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Top Dymeclin Proteins at antibodies-online.com

Showing 7 out of 7 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 39 to 44 Days
$9,248.02
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 39 to 44 Days
$9,248.02
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
Yeast Rat His tag   1 mg Log in to see 56 to 66 Days
$3,956.33
Details
HOST_Escherichia coli (E. coli) Human His tag   100 μg Log in to see 11 to 13 Days
$844.80
Details
HOST_Escherichia coli (E. coli) Human Un-conjugated   100 μg Log in to see 9 to 19 Days
$1,014.95
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 9 to 11 Days
$785.40
Details

DYM Proteins by Origin and Source

Origin Expressed in Conjugate
Human , ,
,
Mouse (Murine)

Rat (Rattus)

More Proteins for Dymeclin (DYM) Interaction Partners

Human Dymeclin (DYM) interaction partners

  1. Dymeclin is crucial for proper myelination and anterograde neuronal trafficking, two processes that are highly active during postnatal brain maturation.

  2. The clinical diagnosis was confirmed with molecular analysis of DYM with a known mutation at c.580C>T (p.R194X).

  3. A novel homozygous splice-site mutation (IVS15+3G>T)of dymeclin gene in the 18q12-12.1 chromosomal region was detected in Dyggve-Melchior-Clausen syndrome.

  4. Data reveal Dymeclin driven processes central to bone development pathways, including Golgi organization, Golgi-coupled protein secretion, and collagen deposition in the extracellular matrix.

  5. dymeclin gene has a role in Golgi function and vesicular transport in the presynapse in schizophrenia in the Japanese population

  6. Gene mutations in a novel, evolutionarily conserved gene are identified in both rare autosomal recessive osteochondrodysplasias (DMC and SMC).

  7. DYM mutations associated with Dyggve-Melchior-Clausen dysplasia result in mis (show AMH Proteins)-localization of Dymeclin.

Mouse (Murine) Dymeclin (DYM) interaction partners

  1. Dymeclin is crucial for proper myelination and anterograde neuronal trafficking, two processes that are highly active during postnatal brain maturation.

Dymeclin (DYM) Protein Profile

Protein Summary

This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation.

Gene names and symbols associated with Dymeclin Proteins (DYM)

  • dymeclin (DYM)
  • dymeclin (TEgg091g12.1)
  • dymeclin (LOC100219344)
  • dymeclin (Dym)
  • dymeclin (dym)
  • 1810041M12Rik protein
  • 4933427L07Rik protein
  • C030019K18Rik protein
  • DMC protein
  • dym protein
  • LOC734107 protein
  • RGD1309111 protein
  • SMC protein

Protein level used designations for Dymeclin Proteins (DYM)

dymeclin , dyggve-Melchior-Clausen syndrome protein

GENE ID SPECIES
455412 Pan troglodytes
698595 Macaca mulatta
734107 Xenopus (Silurana) tropicalis
100053667 Equus caballus
100219344 Taeniopygia guttata
100339069 Oryctolagus cuniculus
100469262 Ailuropoda melanoleuca
100607823 Nomascus leucogenys
54808 Homo sapiens
69190 Mus musculus
291433 Rattus norvegicus
426843 Gallus gallus
446892 Xenopus laevis
100174440 Pongo abelii
480222 Canis lupus familiaris
613923 Bos taurus
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