Gene Symbol | DMWD |
---|---|
Entrez Gene | 1762 |
Alt Symbol | D19S593E, DMR-N9, DMRN9, gene59 |
Species | Human |
Gene Type | protein-coding |
Description | dystrophia myotonica, WD repeat containing |
Other Description | dystrophia myotonica WD repeat-containing protein|dystrophia myotonica-containing WD repeat motif protein|protein 59 |
Swissprots | Q09019 |
Accessions | AAC14447 EAW57386 EAW57387 Q09019 AK309497 BC019266 AAH19266 BC041034 BC156311 AAI56312 BG106514 BM922103 BQ189202 BT006798 AAP35444 BX283745 CD106470 JF432664 ADZ15881 L19267 AAA35767 NM_004943 NP_004934 |
Function | Could have a regulatory function in meiosis. {ECO:0000269|PubMed:8499920}. |
Tissue Specificity | Strongest expression in brain, liver, and testis. Also expressed in kidney and spleen. |