DMP1

GENERAL INFORMATION

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Gene name

DMP1

Gene description

Dentin matrix acidic phosphoprotein 1

Protein class

Disease related genes
Predicted secreted proteins

Predicted localization

Secreted

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Not detected
GTEx:Tissue enriched (testis)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and nuclear expression in several different tissue types.

ANTIBODY RELIABILITY

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Data reliability
description

No RNA expression data detected and pending external verification.

Data reliability

Uncertain based on 1 antibody.
HPA037465
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Not detected

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (testis)

Organ

Expression



GENE INFORMATION

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Gene name

DMP1

Synonyms

Description

Dentin matrix acidic phosphoprotein 1 (HGNC Symbol)

Entrez gene 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]

Chromosome

4

Cytoband

q22.1

Chromosome location (bp)

87650307 - 87664361

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000152592 (version 78.38)

Entrez gene

1758

UniProt

Q13316 (UniProt - Evidence at protein level)

neXtProt

NX_Q13316

Antibodypedia

DMP1 antibodies


PROTEIN BROWSER

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ENST00000282479
 
ENST00000339673
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

DMP1-001 ENSP00000340935
ENST00000339673
Q13316
Show all »
Show » Show » 513 55.8 Yes 0
DMP1-002 ENSP00000282479
ENST00000282479
Q13316
Show all »
Show » Show » 497 54.1 Yes 0