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93145 OLFM2

93145

OLFM2

olfactomedin 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition olfactomedin 2

研究结论

Date Results Publications
2018-10-27 11:26:00 plasma OLFM2 is a potential biomarker for restenosis and may be a novel target for the treatment of restenosis. 29553861
2017-07-01 10:56:00 Our study indicates that OLFM2 is likely to be important in mammalian eye development and disease and should be considered as a gene for human ocular anomalies. 27844144
2015-08-22 10:06:00 Olfm2 physically interacts with serum response factor (SRF) without affecting the SRF-myocardin interaction. 25298399
2010-01-21 00:00:00 The Arg144Gln mutation in OLFM2 is a possible disease-causing mutation in Japanese patients with OAG. Common polymorphisms in OLFM2 and OPTN may interactively contribute to the development of OAG, indicating a polygenic etiology. 17122126
2008-03-13 09:19:00 Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) 17122126

名称对应

Type IDs
Synonymous NOE2, NOELIN2, NOELIN2_V1, OlfC
Gene
UniProtKB-ID: NOE2_HUMAN, K7EIS8_HUMAN
UniprotKB: O95897, K7EIS8
UniParc: UPI0001EED0F1, UPI000013D57B
EMBL: AF131839, AC008752, BC011361, AC008742, BK001428
Ensembl: ENSG00000105088
KO: hsa:93145
Nucleutide sequences
EMBL-CDS: AAD20056.1, AAH11361.1, DAA01550.1
Ensembl_TRS: ENST00000264833, ENST00000590841
Protein sequencees
Ensembl_PRO: ENSP00000264833, ENSP00000464877
RefSeq: NP_001291277.1, NP_477512.1, NP_001291276.1
Others
UniRef100: UniRef100_K7EIS8, UniRef100_O95897
UniRef90: UniRef90_Q568Y7, UniRef90_O95897
UniRef50: UniRef50_O88998, UniRef50_Q568Y7
UniGene: Hs.169743
CCDS: CCDS12221.1

全选

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