Type | Description |
---|---|
Definition | ras homolog family member T1 |
Date | Results | Publications |
---|---|---|
2021-02-27 13:47:00 | Miro: A molecular switch at the center of mitochondrial regulation. | 32056317 |
2020-08-15 18:47:00 | The ROTH1 is a genetic risk factor for Parkinson's disease, further implicating Miro1 in calcium homeostasis and mitochondrial quality control. | 31303019 |
2020-04-04 11:15:00 | circRHOT1 inhibits HCC development and progression via recruiting TIP60 to initiate NR2F6 expression, indicating that circRHOT1 and NR2F6 may be potential biomarkers for HCC prognosis. | 31324186 |
2019-12-28 11:49:00 | Results find that Miro1 is not only a substrate for PINK1/ Parkin-dependent degradation but might also function as a calcium-dependent docking site and safety switch for Parkin recruitment in mitochondria. | 30504269 |
2019-12-07 11:28:00 | Miro1 binds directly to a C-terminal fragment of the Myo19 tail region and that Miro1/2 recruit the Myo19 tail. | 30111583 |
Type | IDs |
---|---|
Synonymous | ARHT1, MIRO-1, MIRO1 |
Gene |
UniProtKB-ID:
MIRO1_HUMAN,
H7BXZ6_HUMAN
UniprotKB:
Q8IXI2,
H7BXZ6
UniParc:
UPI000041E9F7,
UPI000020164E,
UPI0000EE75E2,
UPI0000037C11,
UPI000040B3DA,
UPI000020165E,
UPI000020165D,
UPI0000074394
EMBL:
AC116407,
AK001902,
AY094972,
AC026620,
AJ517412,
CH471147,
BC060781,
AK294407,
AJ496730,
AK022695,
BC068463,
BC015698,
AL136929,
BC041114,
BC051818,
BC125104,
BC125105
Ensembl:
ENSG00000126858
KO:
hsa:55288
|
Nucleutide sequences |
EMBL-CDS:
AAI25105.1,
AAH51818.1,
BAG57659.1,
AAH15698.1,
AAM15734.1,
CAD56956.1,
AAH41114.1,
BAB14185.1,
CAD43139.1,
AAH60781.2,
BAA91969.1,
CAB66863.1,
AAI25106.1,
AAH68463.1,
EAW80251.1
Gene_ORFName:
hCG_1991479
Ensembl_TRS:
ENST00000581094,
ENST00000545287,
ENST00000581031,
ENST00000333942,
ENST00000394692,
ENST00000358365,
ENST00000354266
|
Protein sequencees |
Ensembl_PRO:
ENSP00000351132,
ENSP00000334724,
ENSP00000464094,
ENSP00000378184,
ENSP00000462669,
ENSP00000439737,
ENSP00000346215
RefSeq:
XP_011523271.1,
NP_001275684.1,
XP_016880312.1,
XP_016880308.1,
XP_016880313.1,
XP_024306595.1,
NP_001028738.1,
NP_060777.3,
NP_001275687.1,
XP_011523278.2,
XP_016880309.1,
NP_001028740.1,
XP_011523273.2,
XP_016880314.1,
NP_001275683.1,
XP_011523275.2,
XP_016880311.1,
XP_011523277.1,
XP_016880310.1,
NP_001028739.2
|
Others |
UniRef100:
UniRef100_Q8IXI2
UniRef90:
UniRef90_Q8IXI2
UniRef50:
UniRef50_Q8IXI2
UniGene:
Hs.655325
CCDS:
CCDS74030.1,
CCDS32612.1,
CCDS32610.1,
CCDS32611.1
|
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