Type | Description |
---|---|
Definition | plakophilin 4 |
Date | Results | Publications |
---|---|---|
2013-12-21 11:54:00 | results identify p0071 as an important and novel FMRP target and strongly suggest that impaired actin cytoskeletal functions mediated by an excess of p0071 are key aspects underlying the fragile X syndrome | 24062571 |
2013-04-27 11:19:00 | These data support a model in which dysregulation of the FLCN-p0071 interaction leads to alterations in cell adhesion, cell polarity, and RhoA signaling. | 23139756 |
Type | IDs |
---|---|
Synonymous | 5031422I09Rik, 9430019K17Rik, Armrp, p0071 |
Gene |
UniProtKB-ID:
PKP4_MOUSE,
Q3UIX3_MOUSE,
A2AS47_MOUSE
UniprotKB:
Q68FH0,
Q3UIX3,
A2AS47
UniParc:
UPI0000EE06AF,
UPI000043F2E0,
UPI0000419EC4,
UPI00005AC5A9,
UPI00000EA8FA
EMBL:
BC079848,
BC078638,
BC082578,
AK077250,
AK021168,
AL845536,
BX649232,
AK146720,
AK078240
Ensembl:
ENSMUSG00000026991
KO:
mmu:227937
|
Nucleutide sequences |
EMBL-CDS:
AAH78638.1,
BAC37187.1,
BAC36708.1,
AAH82578.1,
AAH79848.1,
BAB32313.1,
BAE27383.1
Ensembl_TRS:
ENSMUST00000102754,
ENSMUST00000168631,
ENSMUST00000112577
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000129836,
ENSMUSP00000099815,
ENSMUSP00000108196
RefSeq:
XP_036016909.1,
NP_001349919.1,
XP_036016939.1,
XP_036016924.1,
NP_001349923.1,
NP_001349926.1,
XP_036016932.1,
XP_006499238.1,
XP_036016905.1,
XP_036016951.1,
NP_001349922.1,
XP_030106022.1,
NP_001349925.1,
NP_080637.1,
NP_001349924.1,
XP_036016895.1,
XP_036016930.1,
XP_036016943.1,
XP_036016936.1,
NP_780673.2,
XP_036016941.1,
XP_036016937.1,
XP_036016938.1,
XP_036016893.1,
XP_036016888.1,
XP_036016921.1,
XP_036016931.1,
XP_036016897.1,
NP_001349920.1,
XP_036016918.1,
XP_036016915.1,
XP_036016908.1,
XP_030106015.1,
NP_001349921.1,
XP_036016902.1,
XP_036016947.1,
XP_006499235.1,
NP_001349928.1,
NP_001349927.1,
XP_036016889.1,
XP_036016929.1,
XP_036016900.1,
XP_036016953.1,
XP_036016923.1
|
Others |
UniRef100:
UniRef100_Q3UIX3,
UniRef100_Q68FH0
UniRef90:
UniRef90_Q68FH0,
UniRef90_A2AS45
UniRef50:
UniRef50_F1PQ49,
UniRef50_Q68FH0
UniGene:
Mm.260938
CCDS:
CCDS16052.1,
CCDS50588.1
|
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Refseq |
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