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783 CACNB2

783

CACNB2

calcium voltage-gated channel auxiliary subunit beta 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition calcium voltage-gated channel auxiliary subunit beta 2

研究结论

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

名称对应

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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