Type | Description |
---|---|
Definition | nebulin related anchoring protein |
Date | Results | Publications |
---|---|---|
2019-02-09 11:53:00 | Loss-of-function mutation in NRAP gene is associated with dilated cardiomyopathy. | 28611399 |
2010-12-05 22:08:00 | Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) | 20808825 |
2010-06-30 22:05:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
2010-01-21 00:00:00 | Highly conserved and exclusively expressed in cardiac and skeletal muscle. Candidate cause for cardiac and skeletal myopathies | 12789664 |
2009-12-02 21:40:00 | Observational study of gene-disease association. (HuGE Navigator) | 16385451 |
Type | IDs |
---|---|
Synonymous | N-RAP |
Gene |
UniProtKB-ID:
NRAP_HUMAN,
A0A0A0MRM2_HUMAN
UniprotKB:
Q86VF7,
A0A0A0MRM2
UniParc:
UPI0000351D69,
UPI00001F9739,
UPI000264ECBD,
UPI00004589C6,
UPI00004589C7
EMBL:
AL832457,
AK056969,
BC070130,
AF542553,
BC058825,
AK096886,
AL832330,
AL831980,
AY177621,
U96486,
BX640682,
BX641052,
AY177620,
AL832025,
AL390197,
AY081943,
BX640730
Ensembl:
ENSG00000197893
KO:
hsa:4892
|
Nucleutide sequences |
EMBL-CDS:
CAE46027.1,
AAH58825.1,
CAD89998.1,
AAH70130.1,
AAO47074.1,
BAC04884.1,
CAD89910.1,
CAD38623.1,
BAB71328.1,
CAE45811.1,
CAE45846.1,
AAQ09536.1,
AAC51786.1,
CAD89899.1,
AAL99185.2,
AAO47073.1
Ensembl_TRS:
ENST00000359988,
ENST00000360478,
ENST00000369360,
ENST00000369358
|
Protein sequencees |
Ensembl_PRO:
ENSP00000358367,
ENSP00000353666,
ENSP00000353078,
ENSP00000358365
RefSeq:
XP_005269922.1,
XP_011538134.1,
NP_932326.2,
XP_005269921.1,
XP_024303797.1,
NP_001309874.1,
NP_001248392.1,
XP_005269924.1,
XP_006717933.1,
NP_006166.3
|
Others |
UniRef100:
UniRef100_A0A0A0MRM2,
UniRef100_Q86VF7
UniRef90:
UniRef90_G3S2X9,
UniRef90_Q86VF7
UniRef50:
UniRef50_Q86VF7
UniGene:
Hs.268788
CCDS:
CCDS7579.1,
CCDS7578.1
|
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Refseq |
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