DMWD

Aliases
  • D19S593E
  • DM9
  • DMR-N9
  • DMRN9
  • DMWD
  • Dystrophia myotonica-containing WD repeat motif protein
  • Protein 59
  • Protein DMR-N9
  • dystrophia myotonica WD repeat-containing protein
  • dystrophia myotonica, WD repeat containing
  • dystrophia myotonica-containing WD repeat motif
  • dystrophia myotonica-containing WD repeat motif protein
  • gene59
  • protein 59
Description
DMWD is a protein coding gene that is expressed in testis, brain, and 25 other tissues. It is conserved in chimpanzee, dog, cow, mouse, rat, and zebrafish. From NCBI Gene: Predicted to be located in dendrite; nucleus; and perikaryon. [provided by Alliance of Genome Resources, Nov 2021]
Attributes
QA State
Under Review
Type
Gene
HGNC Name
DMWD
Certifications
  • None
QA State for Prostate
Under Review

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.

 Non-Public Biomarker

Organ-specific information for this biomarker is currently being annotated or is "under review". Logging in may give you privileges to view additional information. Contact the Informatics Center if you believe you should have access.