Type | Description |
---|---|
Definition | calcium voltage-gated channel subunit alpha1 E |
Date | Results | Publications |
---|---|---|
2019-05-18 12:18:00 | The variants in CACNA1E as a cause of DEEs. | 30343943 |
2018-01-27 11:11:00 | This study identified a polymorphism in exon 20 of the CACNA1E gene (Asp859Glu - rs35737760) that is more prevalent in hemiplegic and brain stem aura migraine. | 28573794 |
2017-09-09 10:24:00 | Carriers of the minor G allele of the rs3845446 SNP exhibited enhanced pain-related phenotypes after gastrointestinal surgery. The pain-related phenotypes of carriers of the minor allele of this SNP after gastrointestinal surgery were opposite to such phenotypes after orthognathic surgery. | 27480382 |
2015-12-19 10:23:00 | Data suggest that, in vascular smooth muscle cells, increase in cytosolic endothelin-1 (EDN1) induces sustained increase in nuclear Ca2+ via stimulation of R-type calcium channel (CACNA1E) present at the nuclear membrane. | 25741585 |
2014-03-08 12:28:00 | CACNA1E gene single nucleotide polymorphisms may be involved in fentanyl sensitivity. | 23940630 |
Type | IDs |
---|---|
Synonymous | BII, CACH6, CACNL1A6, Cav2.3, EIEE69, gm139 |
Gene |
UniProtKB-ID:
CAC1E_HUMAN,
Q59FG1_HUMAN
UniprotKB:
Q15878,
Q59FG1
UniParc:
UPI00004588C3,
UPI00004588C2,
UPI000044D37D,
UPI00004F6D0F
EMBL:
L29385,
AL160059,
AL590998,
AL161734,
AB209499,
AL359270,
L27745,
L29384
Ensembl:
ENSG00000198216
KO:
hsa:777
|
Nucleutide sequences |
EMBL-CDS:
AAA59205.1,
AAA59204.1,
AAA72125.1,
BAD92736.1
Ensembl_TRS:
ENST00000621551,
ENST00000367570,
ENST00000367573,
ENST00000358338,
ENST00000621791,
ENST00000367567
|
Protein sequencees |
Ensembl_PRO:
ENSP00000356545,
ENSP00000356539,
ENSP00000481619,
ENSP00000351101,
ENSP00000356542,
ENSP00000483914
RefSeq:
XP_016857734.1,
NP_001192222.1,
NP_000712.2,
XP_016857738.1,
XP_016857736.1,
XP_016857732.1,
XP_016857737.1,
NP_001192223.1,
XP_016857740.1,
XP_016857739.1,
XP_016857735.1,
XP_016857733.1
|
Others |
UniRef100:
UniRef100_Q15878,
UniRef100_Q59FG1
UniRef90:
UniRef90_Q59FG1,
UniRef90_Q15878
UniRef50:
UniRef50_Q61290,
UniRef50_Q59FG1
UniGene:
Hs.437444
CCDS:
CCDS55665.1,
CCDS55664.1,
CCDS53443.1
|
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