Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1805
Gene name Gene Name - the full gene name approved by the HGNC.
Dermatopontin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DPT
Synonyms (NCBI Gene) Gene synonyms aliases
TRAMP
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q24.2
Summary Summary of gene provided in NCBI Entrez Gene.
Dermatopontin is an extracellular matrix protein with possible functions in cell-matrix interactions and matrix assembly. The protein is found in various tissues and many of its tyrosine residues are sulphated. Dermatopontin is postulated to modify the be
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs748718975 G>A Pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019412 hsa-miR-148b-3p Microarray 17612493
MIRT944407 hsa-miR-1184 CLIP-seq
MIRT944408 hsa-miR-1205 CLIP-seq
MIRT944409 hsa-miR-1298 CLIP-seq
MIRT944410 hsa-miR-1909 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005201 Function Extracellular matrix structural constituent ISS
GO:0005201 Function Extracellular matrix structural constituent RCA 20551380, 25037231, 27068509, 27559042, 28675934
GO:0005515 Function Protein binding IPI 30082873
GO:0005615 Component Extracellular space HDA 20551380
GO:0007155 Process Cell adhesion IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
125597 3011 ENSG00000143196
Protein
UniProt ID Q07507
Protein name Dermatopontin (Tyrosine-rich acidic matrix protein) (TRAMP)
Protein function Seems to mediate adhesion by cell surface integrin binding. May serve as a communication link between the dermal fibroblast cell surface and its extracellular matrix environment. Enhances TGFB1 activity. Inhibits cell proliferation. Accelerates
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14704 DERM 40 196 Dermatopontin Family
Tissue specificity TISSUE SPECIFICITY: Expressed in fibroblasts, heart, skeletal muscle, brain and pancreas. Expressed at an intermediate level in lung and kidney, and at a low level in liver and placenta. Expressed at a lower level in fibroblasts from hypertrophic scar les
Sequence
Sequence length 201
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Restless Legs Syndrome Restless Legs Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 26683690
Adenoma Associate 24516561
Atrial Fibrillation Associate 23593175
Breast Neoplasms Associate 35819135, 36774339, 39379897
Carcinogenesis Associate 39379897
Cholangiocarcinoma Associate 38300311
Colorectal Neoplasms Associate 24516561, 36012487
Erythema elevatum diutinum Stimulate 36012487
Fibrocartilaginous embolism Associate 33536009
Fibrosis Associate 35159124