DMP1 - dentin matrix acidic phosphoprotein 1 Gene

Also Known as ARHP; ARHR; DMP-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 1758

About DMP1

Cytogenetic location: 4q22.1 Genomic coordinates (GRCh38): 4:87,650,280-87,664,357 (from NCBI)

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

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

  • dentin matrix protein 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
  • ARHR1

  • Arhp

  • Hypophosphatemic Rickets, Ar

  • Arhr

  • Hypophosphatemia, Autosomal Recessive

  • Hypophosphatemia Autosomal Recessive

  • Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets

Hypophosphatemic Rickets, X-Linked Recessive
  • Hypophosphatemic Rickets

  • X-Linked Recessive Hypophosphatemic Rickets

  • XLRHR

  • Hypophosphatemic Rickets Disorders

  • Rickets Hypophosphatemic

  • Rickets, Hypophosphatemic, X-Linked Recessive

  • Familial Hypophosphatemic Rickets

Autosomal Recessive Hypophosphatemic Rickets
  • Arhr

  • Hypophosphatemic Rickets, Autosomal Recessive

  • Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets

Osteomalacia
  • Adult Rickets

Hypophosphatemia
  • Vitamin D-Resistant Rickets

  • Hereditary Hypophosphatemic Rickets

  • Vdrr

  • Vitamin D Resistant Rickets

  • Hypophosphatemic Rickets, X-Linked Dominant

  • Familial Hypophosphatemic Rickets

Rickets
  • Vitamin D Deficiency

  • Vitamin D

  • Active Rickets

  • Hypovitaminosis D

  • Nutritional Rickets

  • Vitamin D Deficiency Disease

  • Vitamin-D Deficiency Rickets

  • Vitamin D-Dependent Rickets

  • Avitaminosis D

  • Infantile Osteomalacia

  • Juvenile Osteomalacia

Dentinogenesis Imperfecta
  • Hereditary Opalescent Dentin

  • Dentinogenesis Imperfecta Without Osteogenesis Imperfecta

  • Dgi

  • Capdepont Teeth

  • Dgi Without Oi

  • Di

  • Non-Syndromic Dgi

  • Non-Syndromic Dentinogenesis Imperfecta

  • Opalescent Teeth Without Oi

  • Opalescent Teeth Without Osteogenesis Imperfecta

  • Opalescent Dentin

Dentinogenesis Imperfecta 1
  • Capdepont Teeth

  • Dentinogenesis Imperfecta Type 2

  • Opalescent Dentin

  • Dentinogenesis Imperfecta Without Osteogenesis Imperfecta

  • Dgi-Ii

  • Dentinogenesis Imperfecta, Shields Type 2

  • DGI1

  • Opalescent Teeth Without Osteogenesis Imperfecta

  • Dentinogenesis Imperfecta, Shields Type Ii

  • Dgi-2

  • Di-2

  • DGI2

  • Dentinogenesis Imperfecta Shields Type Ii

  • Non-Syndromic Dentinogenesis Imperfecta

  • Non-Syndromic Dgi

Dentin Dysplasia
  • Dentinal Dysplasia

  • Dd

  • Dysplasia, Dentin

  • Shell Teeth

Raine Syndrome
  • Lethal Osteosclerotic Bone Dysplasia

  • RNS

  • Renal Nutcracker Syndrome

  • Osteomalacia, Sclerosing, With Cerebral Calcification

  • Left Renal Vein Entrapment Syndrome

  • Csocc

  • Osteosclerotic Bone Dysplasia, Lethal

  • Combination Of Microcephaly, Exophthalmos, Hypoplastic Nose And Midface, Gum Hyperplasia, Cleft Palate, Apparently Low-Set Ears, And Osteosclerosis

  • Nutcracker Syndrome

Vitamin D-Dependent Rickets Type 2b
Nephrolithiasis/Osteoporosis, Hypophosphatemic, 1
  • Hypophosphatemic Nephrolithiasis/Osteoporosis 1

  • NPHLOP1

  • Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1

  • Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 1

Root Resorption
Dental Pulp Necrosis
  • Pulp Necrosis

  • Necrotic Pulp

  • Necrosis Of The Pulp

  • Dead Pulp

  • Devitalised Pulp

  • Putrescent Pulpitis

  • Devitalized Tooth

  • Dental Pulp Gangrene

  • Pulp Gangrene

  • Nonvital Tooth

  • Pulpless Tooth

  • Putrescent Pulp

Fanconi Renotubular Syndrome 2
  • FRTS2

  • Fanconi Renotubular Syndrome, Type 2

Hypophosphatemic Nephrolithiasis/Osteoporosis
  • Nephrolithiasis/Osteoporosis, Hypophosphatemic

Sclerosteosis 1
  • SOST1

  • Sost

  • Cortical Hyperostosis With Syndactyly

  • Sclerosteosis

  • Sclerosteosis, Type 1

Osteoglophonic Dysplasia
  • Osteoglophonic Dwarfism

  • OGD

  • Fairbank-Keats Syndrome

  • Osteoglosphonic Dysplasia

  • Dysplasia, Osteoglophonic

Dental Caries
  • Dental Caries Extending Into Pulp

  • Dental Caries Of Smooth Surface

  • Dental Caries Pit And Fissure

  • Smooth Surface Dental Caries

  • Dental Decay

  • Carious Teeth

  • Dental Cavity

  • Saprodontia

  • Teeth Decayed

  • Tooth Caries

  • Tooth Decay

Dental Pulp Disease
  • Dental Pulp Diseases

  • Dental Pulp Disorder

  • Disorder Of Pulp Of Tooth

  • Pulp Disorder

Hypophosphatemic Rickets, Autosomal Dominant
  • Autosomal Dominant Hypophosphatemic Rickets

  • ADHR

  • Autosomal Dominant Hypophosphatemia

  • Vitamin D-Resistant Rickets, Autosomal Dominant

  • Hypophosphatemia, Autosomal Dominant

  • Autosomal Dominant Vitamin D-Resistant Rickets

  • Rickets, Hypophosphatemic, Autosomal Dominant

Vitamin D Hydroxylation-Deficient Rickets, Type 1b
  • VDDR1B

  • Vitamin D-Dependent Rickets Type 1b

  • Vitamin D-Dependent Rickets, Type 1b

  • 25-Hydroxyvitamin D3 Deficiency, Selective

  • Pseudovitamin D3 Deficiency Rickets Due To 25-Hydroxylase Deficiency

  • Rickets Due To Defect In Vitamin D 25-Hydroxylation Deficiency

  • Rickets Vitamin D-Dependent 1b

  • 25-Hydroxyvitamimn D3 Deficiency Selective

  • 25-Hydroxyvitamin D(3) Deficiency

  • Pseudovitamin D(3) Deficiency Rickets Due To 25-Hydroxylase Deficiency

  • Selective 25-Hydroxyvitamin D(3) Deficiency

  • Rickets Due To Defect In Vitamin D 25-Hydroxylation

Hypophosphatemic Rickets, X-Linked Dominant
  • X-Linked Hypophosphatemia

  • Xlh

  • Vitamin D-Resistant Rickets, X-Linked

  • X-Linked Hypophosphatemic Rickets

  • XLHR

  • Hyp

  • Hypophosphatemic Vitamin D-Resistant Rickets

  • Hpdr

  • X-Linked Dominant Hypophosphatemic Rickets

  • Familial Hypophosphatemic Rickets

  • Hypophosphatemia, X-Linked

  • Hypophosphatemia, Vitamin D-Resistant Rickets

  • Hypophosphatemic Rickets X-Linked Dominant

  • X-Linked Vitamin D-Resistant Rickets

  • Hypophophatemia, X-Linked

  • Hypophophatemic Vitamin D-Resistant Rickets

  • Hypophosphatemia X-Linked

  • Vitamin D-Resistant Rickets X-Linked

  • Vitamin D-Resistant Rickets

  • Rickets, X-Linked Hypophosphatemic

Vitamin D Hydroxylation-Deficient Rickets, Type 1a
  • Vitamin D-Dependent Rickets, Type 1a

  • Vitamin D-Dependent Rickets, Type 1

  • VDDR1A

  • 25-Hydroxycholecalciferol-1-Hydroxylase Deficiency

  • 1-Alpha-Hydroxylase Deficiency

  • Vdd1

  • Pddr1a

  • Pddr Ia

  • Vitamin D-Dependent Rickets, Type I

  • Vitamin D-Dependent Rickets Type 1a

  • 1-Alpha, 25-Hydroxyvitamin D3 Deficiency, Selective

  • Vitamin D Dependency, Type 1

  • Pseudovitamin D-Deficiency Rickets, Type Ia

  • Rickets Vitamin D-Dependent 1a

  • 1-Alpha 25-Hydroxyvitamin D3 Deficiency Selective

  • Pddr

  • Pseudovitamin D Deficiency Rickets

  • Pseudovitamin D-Deficiency Rickets Type Ia

  • Vitamin D Dependency Type 1

Familial Isolated Hypoparathyroidism
  • Fih

Arterial Calcification Of Infancy
  • Idiopathic Infantile Arterial Calcification

  • Generalized Arterial Calcification Of Infancy

  • Iiac

  • Occlusive Infantile Arteriopathy

  • Infantile Arteriosclerosis

  • Gaci

  • Idiopathic Obliterative Arteriopathy

  • Generalized Arterial Calcification In Infancy

  • Arteriopathia Calcificans Infantum

  • Diffuse Arterial Calcifying Elastopathy Of Infancy

  • Infantile Calcifying Arteriopathy

  • Medial Coronary Sclerosis Of Infancy

  • Coronary Sclerosis, Medial, Of Infancy

  • Calcification, Arterial, Generalized, Infancy

Dental Abscess
Vitamin D-Dependent Rickets, Type 2a
  • Hvdrr

  • Generalized Resistance To 1,25-Dihydroxyvitamin D

  • Hypocalcemic Vitamin D-Resistant Rickets

  • VDDR2A

  • Rickets, Hereditary Vitamin D-Resistant

  • Vitamin D-Resistant Rickets With End-Organ Unresponsiveness To 1,25-Dihydroxycholecalciferol

  • Pddr Iia

  • Rickets-Alopecia Syndrome

  • Rickets, Vitamin D-Resistant, Type Iia

  • Vitamin D-Dependent Rickets Type 2a

  • Vitamin D-Dependent Rickets, Type 2

  • Vitamin D-Dependent Rickets, Type 2a, With Or Without Alopecia

  • Generalized 1,25-Dihydroxyvitamin D

  • Pseudovitamin D-Deficiency, Type Iia

  • Hereditary Vitamin D-Resistant Rickets

  • Vddr Ii

  • Vdrr Ii

  • Vitamin D-Dependent Rickets Type Ii

  • Vitamin D-Resistant Rickets Type Ii

  • Rickets Vitamin D-Dependent 2a

  • Pseudovitamin D-Deficiency Type Iia

  • Rickets Hereditary Vitamin D-Resistant

  • Type Iia Rickets

  • Vitamin D-Dependent Rickets Type 2a With Or Without Alopecia

  • Vitamin D-Dependent Rickets, Type Ii

  • Familial Hypophosphatemic Rickets

  • Hypophosphatemic Rickets, X-Linked Dominant

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

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