Type | Description |
---|---|
Definition | EYA transcriptional coactivator and phosphatase 1 |
Date | Results | Publications |
---|---|---|
2020-06-06 10:08:00 | LINC00511 interacted with EYA1 promoted HCC development via mediating miR-195, proposing a promising therapeutic biomarker for HCC diagnosis and prognosis. | 31731191 |
2019-11-02 12:30:00 | Results supported the heterogeneity of the genetic and phenotypic spectrum of Branchio-Oto syndrome. The recurrent c.967-2A>G in different ethnical groups suggested that it is a hot-spot mutation. | 31102969 |
2019-04-27 10:18:00 | Protein Eya1 is essential in regulating cancer cell-mediated angiogenesis and contributes to tumor growth. | 29496520 |
2019-04-20 12:12:00 | The affected members harbored a novel heterozygous nonsense variation in exon 11 of EYA1. | 30086703 |
2018-09-01 10:55:00 | SIX1/EYA1 mutations might be partially responsible for conotruncal heart defects. | 29043394 |
Type | IDs |
---|---|
Synonymous | BOP, BOR, BOS1, OFC1 |
Gene |
UniProtKB-ID:
EYA1_HUMAN,
A0A2R8Y6K4_HUMAN,
A6NCB9_HUMAN,
Q0P517_HUMAN,
F8WB53_HUMAN,
A0A024R813_HUMAN,
B3KXR1_HUMAN
UniprotKB:
Q99502,
A0A2R8Y6K4,
A6NCB9,
Q0P517,
F8WB53,
A0A024R813,
B3KXR1
UniParc:
UPI000155D697,
UPI000155D699,
UPI000012A3B3,
UPI000002A936,
UPI000013F3DF,
UPI000387C40C,
UPI00004A28B5,
UPI0000DBEBB5
EMBL:
AC099805,
BC121798,
BC121799,
AK295897,
AF467247,
AJ000097,
AK127798,
AJ000098,
AC016465,
AC022858,
AC009446,
Y10260,
CH471068
Ensembl:
ENSG00000104313
KO:
hsa:2138
|
Nucleutide sequences |
EMBL-CDS:
CAA03922.1,
CAA03923.1,
EAW86976.1,
CAA71309.1,
AAL73437.1,
AAI21800.1,
BAG58690.1,
AAI21799.1,
EAW86979.1,
EAW86980.1,
BAG54573.1
Gene_ORFName:
hCG_17379
Ensembl_TRS:
ENST00000388742,
ENST00000388740,
ENST00000419131,
ENST00000340726,
ENST00000647540,
ENST00000645793,
ENST00000643681,
ENST00000303824,
ENST00000388743
|
Protein sequencees |
Ensembl_PRO:
ENSP00000373394,
ENSP00000496255,
ENSP00000494438,
ENSP00000410176,
ENSP00000342626,
ENSP00000373392,
ENSP00000495390,
ENSP00000303221,
ENSP00000373395
RefSeq:
XP_016868691.1,
NP_001357264.1,
XP_016868692.1,
NP_742055.1,
XP_016868693.1,
NP_001275504.1,
XP_016868702.1,
NP_000494.2,
NP_001275503.1,
NP_001357262.1,
XP_011515786.2,
XP_016868694.1,
XP_016868696.1,
NP_001357263.1,
XP_016868701.1,
XP_016868697.1,
XP_016868700.1,
XP_011515785.1,
NP_742056.2,
NP_001357265.1
|
Others |
UniRef100:
UniRef100_B3KXR1,
UniRef100_Q0P517,
UniRef100_F8WB53,
UniRef100_A6NCB9,
UniRef100_Q99502
UniRef90:
UniRef90_B3KXR1,
UniRef90_P97767,
UniRef90_Q0P517,
UniRef90_Q99502
UniRef50:
UniRef50_P97767,
UniRef50_Q99502,
UniRef50_F1ND27,
UniRef50_O00167-3
UniGene:
Hs.491997
CCDS:
CCDS34906.1
|
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