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805 CALM2

805

CALM2

calmodulin 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition calmodulin 2

研究结论

Date Results Publications
2021-04-17 13:18:00 Targeting CALM2 Inhibits Hepatocellular Carcinoma Growth and Metastasis by Suppressing E2F5-mediated Progression. 33788723
2020-04-25 11:24:00 Liver fibrosis caused by hepatitis C virus results in down-regulation of hepatic CALM2 expression. 30317608
2019-10-12 13:10:00 Protein molecular diagnosis of autosomal dominant calmodulin mutations causing irregular heart rhythms has been presented. 29932249
2019-09-21 11:08:00 Novel Association of a CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy. 30354306
2017-12-23 12:33:00 Impaired Ca(2+)-dependent inactivation in human cardiomyocytes as the plausible mechanism for Long QT Syndrome associated with 2 novel CaM mutations. 27374306

名称对应

Type IDs
Synonymous CALM, CALML2, CAM1, CAM3, CAMC, CAMII, CAMIII, LQT15, PHKD, PHKD2, caM
Gene
UniProtKB-ID: CALM3_HUMAN, CALM2_HUMAN, CALM1_HUMAN, Q96HY3_HUMAN, B4DJ51_HUMAN
UniprotKB: P0DP25, P0DP24, P0DP23, Q96HY3, B4DJ51
UniParc: UPI0000073822, UPI00000000C1
EMBL: X52608, M19311, BC026065, CH471061, BC018677, CH471126, U11886, BC000454, CH471053, M27319, U94726, AK295927, BC011834, X52606, BC003354, AC006536, BT006818, X52607, J04046, U12022, BC017385, CR542021, AY189287, AC073283, FJ224310, BT009916, U94725, BT006855, U94728, BC005137, BC008437, BC008597, CR541990, BC007965, AC093503, AL512791, BC006464, BC047523, D45887
Ensembl: ENSG00000160014, ENSG00000143933, ENSG00000198668
KO: hsa:801, hsa:805, hsa:808
Nucleutide sequences
EMBL-CDS: AAP35501.1, AAA51918.1, CAA36839.1, AAH05137.1, AAA35641.1, CAG46787.1, AAH08437.1, AAC83174.1, AAH03354.1, AAY24085.1, AAH18677.1, AAH17385.1, CAG46818.1, AAH26065.1, AAP88918.1, AAH06464.1, BAA08302.1, AAD45181.1, AAH00454.1, AAA35635.1, AAB60644.1, AAH11834.1, AAP35464.1, AAH08597.1, EAX00221.1, EAW57425.1, AAO86731.1, EAX00222.1, EAX00223.1, EAX00220.1, AAH07965.1, EAW57426.1, EAW81427.1, ACI46002.1, EAW81428.1, BAG58713.1
Gene_ORFName: hCG_17033, hCG_20313, hCG_21749, hCG_20313
Ensembl_TRS: ENST00000596362, ENST00000291295, ENST00000272298, ENST00000654798, ENST00000356978, ENST00000663135, ENST00000659177, ENST00000456319, ENST00000447653, ENST00000655728, ENST00000655450, ENST00000553542, ENST00000656538, ENST00000544280, ENST00000598871, ENST00000599839, ENST00000391918, ENST00000594523, ENST00000668667
Protein sequencees
Ensembl_PRO: ENSP00000472141, ENSP00000291295, ENSP00000499797, ENSP00000272298, ENSP00000349467, ENSP00000499266, ENSP00000499357, ENSP00000499656, ENSP00000471225, ENSP00000403491, ENSP00000499498, ENSP00000468877, ENSP00000442853, ENSP00000375785, ENSP00000411440, ENSP00000499706, ENSP00000470502, ENSP00000499421, ENSP00000450829
RefSeq: NP_001292553.1, NP_001734.1, NP_001292555.1, NP_001292554.1
Others
UniRef100: UniRef100_P0DP23
UniRef90: UniRef90_P0DP23
UniRef50: UniRef50_P0DP23
UniGene: Hs.468442
CCDS: CCDS33061.1, CCDS86782.1, CCDS1832.1, CCDS9892.1

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