| 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.
|