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491 ATP2B2

491

ATP2B2

ATPase plasma membrane Ca2+ transporting 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition ATPase plasma membrane Ca2+ transporting 2

研究结论

Date Results Publications
2019-09-07 12:19:00 A V1143F substitution in PMAC2 alters the binding of caslmodulin to the calmodulin-binding domain leading to impaired calcium signaling. 29655659
2019-02-23 13:33:00 PMCA2 loss plays a role in the ataxic phenotype, but can paradoxically also minimise calcium rises in cerebellar Purkinje neurons, thereby ensuring their resilience and survival. 29452612
2019-02-23 13:33:00 critical role played by the PMCA2w/a pump in the control of hair cell function and survival, and provide mechanistic insight into the etiology of deafness and vestibular disorders. 29452611
2019-02-16 11:20:00 Loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. 30535804
2018-02-17 11:45:00 PMCA2 regulates breast cancer cell proliferation and sensitivity to doxorubicin in basal cell carcinoma. 27148852

名称对应

Type IDs
Synonymous PMCA2, PMCA2a, PMCA2i
Gene
UniProtKB-ID: AT2B2_HUMAN, A0A024R2E4_HUMAN, Q4LE63_HUMAN
UniprotKB: Q01814, A0A024R2E4, Q4LE63
UniParc: UPI00001261EF, UPI000002A445, UPI000002A441, UPI000054C91A, UPI000002A444, UPI0000E08117, UPI000002A442, UPI0001FDB7F8, UPI000002A443
EMBL: U15688, AC018839, L00620, X63575, L20977, M97260, AB210008, CH471055, AC090841
Ensembl: ENSG00000157087
KO: hsa:491
Nucleutide sequences
EMBL-CDS: AAA36456.1, CAA45131.1, AAA60985.1, AAA51893.1, AAA50877.1, EAW64082.1, EAW64079.1, BAE06090.1
Gene_ORFName: hCG_1811446
Ensembl_TRS: ENST00000397077, ENST00000646379, ENST00000643662, ENST00000644807, ENST00000360273, ENST00000452124, ENST00000460129, ENST00000645850
Protein sequencees
Ensembl_PRO: ENSP00000495924, ENSP00000495228, ENSP00000494716, ENSP00000414854, ENSP00000424494, ENSP00000494381, ENSP00000353414, ENSP00000380267
RefSeq: XP_016861978.1, XP_016861976.1, NP_001674.2, XP_016861973.1, NP_001350791.1, XP_016861981.1, NP_001317540.1, XP_006713238.1, XP_016861972.1, XP_016861974.1, XP_016861971.1, XP_016861977.1, NP_001340493.1, XP_016861970.1, XP_011532054.1, XP_016861975.1, XP_005265236.1, NP_001001331.1
Others
UniRef100: UniRef100_A0A024R2E4, UniRef100_Q01814
UniRef90: UniRef90_A0A024R2E4, UniRef90_Q01814
UniRef50: UniRef50_Q01814-3, UniRef50_Q9R0K7
UniGene: Hs.268942
CCDS: CCDS82733.1, CCDS33701.1, CCDS2601.1

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