Type | Description |
---|---|
Definition | calcium voltage-gated channel auxiliary subunit beta 2 |
Date | Results | Publications |
---|---|---|
2021-02-20 13:28:00 | CACNB2 rs11013860 polymorphism correlates of prefrontal cortex thickness in bipolar patients with first-episode mania. | 32158010 |
2021-01-09 13:26:00 | Autism-associated mutations in the CaVbeta2 calcium-channel subunit increase Ba(2+)-currents and lead to differential modulation by the RGK-protein Gem. | 31887354 |
2020-03-21 11:38:00 | Our data show that L-type calcium channels regulate VEGF expression and secretion from retinal pigment epithelial cells and support the role of CACNB2 via regulation of VEGF in the pathogenesis of proliferative diabetic retinopathy. | 31439644 |
2019-12-14 11:56:00 | Our study demonstrates that bipolar disorder patients with the CACNB2 rs11013860 AA/CA genotype may exhibit altered hippocampal-cortical connectivity. | 30744588 |
2019-10-26 10:28:00 | The results indicate that CACNB2 gene polymorphism was significantly associated with higher odds of high blood pressure in Lithuanian adolescents aged 12-15 years. | 29982197 |
Type | IDs |
---|---|
Synonymous | CACNLB2, CAVB2, MYSB |
Gene |
UniProtKB-ID:
CACB2_HUMAN,
Q5VVH1_HUMAN,
Q59H42_HUMAN,
A0A494C0B2_HUMAN,
A0A494C184_HUMAN
UniprotKB:
Q08289,
Q5VVH1,
Q59H42,
A0A494C0B2,
A0A494C184
UniParc:
UPI0003EAED45,
UPI00004F6AD1,
UPI0000141420,
UPI00029DB971,
UPI00001F8FC3,
UPI000034ECDF,
UPI000036666C,
UPI000022892B,
UPI0000458872,
UPI00015294AD,
UPI0000141429,
UPI000036666B,
UPI00001AEA80
EMBL:
AL450384,
AY027893,
CH471072,
AL450364,
AY027894,
AY027895,
AF285239,
AY027896,
AY393858,
AF137377,
AL139814,
AY027898,
AY393860,
AF423190,
AL360231,
U95019,
AY027897,
AK299873,
AF423189,
AY393859,
AL353603,
AF465485,
BC136409,
AY393861,
AF137376,
AL390783,
AY393862,
S60415,
AB208917,
AF423192,
AF423191
Ensembl:
ENSG00000165995
KO:
hsa:783
|
Nucleutide sequences |
EMBL-CDS:
AAQ97606.1,
AAL73495.1,
EAW86197.1,
AAB53332.1,
AAD33730.1,
AAQ97607.1,
AAB51370.1,
AAQ97610.1,
AAD33729.1,
AAL16950.1,
AAG01473.2,
AAK16994.1,
AAI36410.1,
AAL16948.1,
AAL16949.1,
EAW86196.1,
AAQ97609.1,
AAL16951.1,
AAQ97608.1,
BAH13158.1,
BAD92154.1
Ensembl_TRS:
ENST00000324631,
ENST00000377329,
ENST00000282343,
ENST00000645287,
ENST00000352115,
ENST00000377319,
ENST00000377315,
ENST00000396576,
ENST00000650685,
ENST00000652391
|
Protein sequencees |
Ensembl_PRO:
ENSP00000282343,
ENSP00000366536,
ENSP00000496203,
ENSP00000366546,
ENSP00000344474,
ENSP00000366532,
ENSP00000320025,
ENSP00000379821,
ENSP00000498460,
ENSP00000498938
RefSeq:
NP_963866.2,
XP_006717565.1,
NP_963887.2,
NP_963884.2,
XP_011517961.1,
XP_016872114.1,
NP_963865.2,
XP_005252648.1,
NP_963890.2,
NP_963891.1,
NP_963864.1,
NP_000715.2,
NP_001161417.1,
XP_005252645.1,
NP_001316989.1
|
Others |
UniRef100:
UniRef100_A0A494C184,
UniRef100_A0A494C0B2,
UniRef100_Q08289-2,
UniRef100_Q5VVH1,
UniRef100_Q08289
UniRef90:
UniRef90_Q08289,
UniRef90_Q08289-2
UniRef50:
UniRef50_Q08289
UniGene:
Hs.59093
CCDS:
CCDS7126.1,
CCDS41493.1,
CCDS7127.1,
CCDS7129.1,
CCDS41494.1,
CCDS81442.1,
CCDS7128.1,
CCDS7125.1
|
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