DMP1 - dentin matrix acidic phosphoprotein 1 Gene
Also Known as ARHP; ARHR; DMP-1
Species: Homo sapiens
About DMP1
This gene has 7 transcripts (splice variants), 109 orthologues and is associated with 3 phenotypes. Low expression observed in reference dataset.
Summary
Dentin matrix acidic phosphoprotein is an extracellular matrix protein and a member of the small Integrin binding ligand N-linked glycoprotein family. This protein, which is critical for proper mineralization of bone and dentin, is present in diverse cells of bone and tooth tissues. The protein contains a large number of acidic domains, multiple phosphorylation sites, a functional arg-gly-asp cell attachment sequence, and a DNA binding domain. In undifferentiated osteoblasts it is primarily a nuclear protein that regulates the expression of osteoblast-specific genes. During osteoblast maturation the protein becomes phosphorylated and is exported to the extracellular matrix, where it orchestrates mineralized matrix formation. Mutations in the gene are known to cause autosomal recessive hypophosphatemia, a disease that manifests as rickets and osteomalacia. The gene structure is conserved in mammals. Two transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
DMP1 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001079911.3 | NP_001073380.1 | dentin matrix acidic phosphoprotein 1 isoform 2 precursor |
| NM_004407.4 | NP_004398.1 | dentin matrix acidic phosphoprotein 1 isoform 1 precursor |
DMP1 Protein Structure
DMP1: Dentin matrix protein 1 (DMP1) (1 - 513)
- 0
- 100
- 200
- 300
- 400
- 513 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
dentin matrix acidic phosphoprotein 1 |
|
Recombinant DMP1 Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P70105 | DMP-1 Protein, Human (HEK293, His) | Q13316 (L17-Y513) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Hypophosphatemic Rickets, Autosomal Recessive, 1 |
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| Hypophosphatemic Rickets, X-Linked Recessive |
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| Autosomal Recessive Hypophosphatemic Rickets |
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| Osteomalacia |
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| Hypophosphatemia |
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| Rickets |
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| Dentinogenesis Imperfecta |
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| Dentinogenesis Imperfecta 1 |
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| Dentin Dysplasia |
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| Raine Syndrome |
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| Vitamin D-Dependent Rickets Type 2b |
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| Nephrolithiasis/Osteoporosis, Hypophosphatemic, 1 |
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| Root Resorption |
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| Dental Pulp Necrosis |
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| Fanconi Renotubular Syndrome 2 |
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| Hypophosphatemic Nephrolithiasis/Osteoporosis |
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| Sclerosteosis 1 |
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| Osteoglophonic Dysplasia |
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| Dental Caries |
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| Dental Pulp Disease |
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| Hypophosphatemic Rickets, Autosomal Dominant |
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| Vitamin D Hydroxylation-Deficient Rickets, Type 1b |
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| Hypophosphatemic Rickets, X-Linked Dominant |
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| Vitamin D Hydroxylation-Deficient Rickets, Type 1a |
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| Familial Isolated Hypoparathyroidism |
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| Arterial Calcification Of Infancy |
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| Dental Abscess |
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| Vitamin D-Dependent Rickets, Type 2a |
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Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Canis familiaris | DMP1 | VGNC | VGNC:57414 |
| Mus musculus | DMP1 | MGD | MGI:94910 |
| Rattus norvegicus | DMP1 | RGD | RGD:2508 |
| Felis catus | DMP1 | VGNC | VGNC:107327 |
| Macaca mulatta | DMP1 | VGNC | VGNC:71933 |
| Bos taurus | DMP1 | VGNC | VGNC:28108 |
| Others | DMP1 | NCBI |