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4892 NRAP

4892

NRAP

nebulin related anchoring protein

protein-coding

Homo sapiens

基因描述

Type Description
Definition nebulin related anchoring protein

研究结论

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

名称对应

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

全选

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