Type | Description |
---|---|
Definition | lamin A |
Date | Results | Publications |
---|---|---|
2021-03-13 13:27:00 | Identification of Genes and Pathways Regulated by Lamin A in Heart. | 32805188 |
2021-02-27 13:53:00 | Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular Dystrophy. | 32244403 |
2021-02-27 13:50:00 | Consequences of Lmna Exon 4 Mutations in Myoblast Function. | 32455813 |
2021-02-13 13:24:00 | Mutated lamin A modulates stiffness in muscle cells. | 32540097 |
2021-02-02 13:22:00 | Dysfunctional polycomb transcriptional repression contributes to lamin A/C-dependent muscular dystrophy. | 31999646 |
Type | IDs |
---|---|
Synonymous | Dhe |
Gene |
UniProtKB-ID:
LMNA_MOUSE
UniprotKB:
P48678
UniParc:
UPI0000023EF0,
UPI0000029392,
UPI00000279E2
EMBL:
AK150624,
AK150391,
D14850,
BC094020,
DQ832702,
AK152539,
AK147150,
AK149998,
AK150501,
AK161221,
AK152846,
BC015302,
CH466547,
AK004619,
D13181,
AK152646,
AK167858,
X14170,
D49733,
DQ832703
Ensembl:
ENSMUSG00000028063
KO:
mmu:16905
|
Nucleutide sequences |
EMBL-CDS:
BAE29614.1,
BAE36246.1,
BAB23415.1,
BAA08570.1,
AAH94020.1,
BAA08569.1,
BAE27717.1,
BAA02476.1,
BAA03578.1,
BAE31384.1,
ABI16252.1,
BAA08571.1,
CAA32372.1,
EDL15275.1,
AAH15302.1,
BAE29714.1,
BAE29226.1,
BAE39876.1,
BAE31294.1,
ABI16251.1,
BAE29519.1,
BAE31539.1
Ensembl_TRS:
ENSMUST00000036252,
ENSMUST00000029699,
ENSMUST00000120377
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000029699,
ENSMUSP00000040265,
ENSMUSP00000113093
RefSeq:
NP_001104572.1,
NP_001002011.2,
NP_062263.1,
XP_006501136.1
|
Others |
UniRef100:
UniRef100_P48678
UniRef90:
UniRef90_P48678
UniRef50:
UniRef50_P02545
UniGene:
Mm.243014,
Mm.471227
CCDS:
CCDS50951.1,
CCDS38482.1,
CCDS38483.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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