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55203 LGI2

55203

LGI2

leucine rich repeat LGI family member 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition leucine rich repeat LGI family member 2

研究结论

Date Results Publications
2011-01-15 11:16:00 The similarity of LGI2 share a common molecular disease mechanism causing genotypically distinct but phenotypically related forms of epilepsy. 20863412
2010-06-28 11:07:00 protein sequence analysis and patient-specific chromosomal deletions are provided for LGI2 as the prime candidate gene for partial epilepsy with pericentral spikes among the 52 genes known at locus 4p15 20183877

名称对应

Type IDs
Synonymous LGIL2
Gene
UniProtKB-ID: LGI2_HUMAN
UniprotKB: Q8N0V4
UniParc: UPI0000047256
EMBL: AF467955, BC101759, AJ487958, BC101761, AB067503, AK001537, AJ487516
Ensembl: ENSG00000153012
KO: hsa:55203
Nucleutide sequences
EMBL-CDS: BAA91746.1, AAI01762.1, AAI01760.1, CAD32305.1, CAD31784.1, BAB67809.1, AAM49553.1
Ensembl_TRS: ENST00000382114
Protein sequencees
Ensembl_PRO: ENSP00000371548
RefSeq: XP_011512152.1, XP_016863845.1, NP_060646.2
Others
UniRef100: UniRef100_Q8N0V4
UniRef90: UniRef90_Q8K4Z0
UniRef50: UniRef50_Q8K4Z0
UniGene: Hs.12488
CCDS: CCDS3431.1

全选

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研究热度

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