Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Expr. PhenotypesPheno. Gene Literature (17)Lit. (17) GO Terms (127)GO (127) Nucleotides (189)Nucl. (189) Proteins (97)Prot. (97) Interactants (218)Interact. (218) Wiki
XB-GENEPAGE-5813246
???displayGene.symbol???:
 dmd

???displayGene.name???: 
dystrophin, gene 1

???displayGene.synonyms???
dmd.1 , dystrophin , utrn ( Nomenclature history )

???displayGene.geneFunction???
actin binding

AI Protein Function :
dmd is a large cytoskeletal protein that links actin filaments to the dystrophin‑glycoprotein complex at the sarcolemma, providing membrane stability during muscle contraction. It functions as a struct...[+]


???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
non-syndromic X-linked intellectual disability [+]

MIM:
MUSCULAR DYSTROPHY, BECKER TYPE; BMD [+]

External Links:
Loading gene data...
Please wait while we fetch the latest information
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:
???displayGene.mophenotype???
???displayGene.mosmith??? tneu143c03      


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info