Type | Description |
---|---|
Definition | myelin regulatory factor |
Date | Results | Publications |
---|---|---|
2021-03-13 13:20:00 | Pancreatic Require the MYRF to Maintain ER Homeostasis. | 32997974 |
2020-12-12 13:24:00 | Functional mechanism and pathogenic potential of MYRF ICA domain mutations implicated in birth defects. | 31964908 |
2020-07-11 11:33:00 | results underline the importance of including SLC18A3 sequencing in the differential diagnostics of fetuses with arthrogryposis, FADS, or LMPS of unknown etiology | 31069960 |
2020-04-25 12:43:00 | C-terminal variants in MYRF, which are expected to escape nonsense-mediated decay, represent a rare cause of autosomal dominant nanophthalmos with or without dextrocardia or congenital diaphragmatic hernia. | 31700225 |
2020-03-14 10:46:00 | The results suggest that MYRF is a novel causative gene of 46,XY and 46,XX disorders of sex development and MYRF is a transcription factor regulating coelomic epithelium and/or coelomic epithelium derived cells proliferation and migration, which is essential for development of multiple organs. | 30985895 |
Type | IDs |
---|---|
Synonymous | 11orf9, C11orf9, CUGS, MMERV, MRF, Ndt80, pqn-47 |
Gene |
UniProtKB-ID:
MYRF_HUMAN
UniprotKB:
Q9Y2G1
UniParc:
UPI00000720D3,
UPI0000D45F7B
EMBL:
AF038536,
AF086762,
AB023171,
CH471076
Ensembl:
ENSG00000124920
KO:
hsa:745
|
Nucleutide sequences |
EMBL-CDS:
BAA76798.2,
EAW73968.1,
AAF28400.1,
AAB92668.1
Ensembl_TRS:
ENST00000265460,
ENST00000278836
|
Protein sequencees |
Ensembl_PRO:
ENSP00000265460,
ENSP00000278836
RefSeq:
XP_011543536.1,
XP_005274285.1,
XP_005274282.1,
NP_001120864.1,
XP_005274284.1,
NP_037411.1,
XP_024304445.1,
XP_005274281.1,
XP_005274280.1,
XP_005274279.1,
XP_005274283.1
|
Others |
UniRef100:
UniRef100_Q9Y2G1
UniRef90:
UniRef90_Q9Y2G1
UniRef50:
UniRef50_Q3UR85-3
UniGene:
Hs.473109
CCDS:
CCDS44622.1,
CCDS31579.1
|
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Refseq |
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