Type | Description |
---|---|
Definition | calmodulin 2 |
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 |
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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Refseq |
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