Type | Description |
---|---|
Definition | leucine rich repeat and fibronectin type III domain containing 2 |
Date | Results | Publications |
---|---|---|
2020-02-15 10:04:00 | No significant association of variant rs2494938 of LRFN2 was observed with ovarian canceror breast cancer in a cohort of women in India. | 31605628 |
2019-10-05 10:31:00 | study demonstrated that the polymorphisms rs2494938 at 6p21.1 and rs2285947 at 7p15.3 may serve as independent prognostic biomarkers for ESCC, implying the potential biological role of their related genes (LRFN2 and DNAH11) in the process of ESCC development | 31053115 |
2017-07-29 12:42:00 | Microdeletion encompassing LRFN2 gene segregates with working memory deficits and learning disabilities in three family members. | 26486473 |
2012-04-21 12:02:00 | enrichment of SALM1 on the cell surface affects dendritic arborization, and intracellular motifs regulate its dendritic versus axonal localization. | 22174418 |
2010-06-30 22:05:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
Type | IDs |
---|---|
Synonymous | FIGLER2, KIAA1246, SALM1 |
Gene |
UniProtKB-ID:
LRFN2_HUMAN
UniprotKB:
Q9ULH4
UniParc:
UPI00001C1E47
EMBL:
AB033072,
AL591063,
AK291474,
BC142616,
CH471081
Ensembl:
ENSG00000156564
KO:
hsa:57497
|
Nucleutide sequences |
EMBL-CDS:
AAI42617.1,
EAX04006.1,
BAA86560.1,
BAF84163.1
Ensembl_TRS:
ENST00000338305
|
Protein sequencees |
Ensembl_PRO:
ENSP00000345985
RefSeq:
XP_016866600.1,
NP_065788.1,
XP_011513064.1,
XP_016866599.1,
XP_011513063.1
|
Others |
UniRef100:
UniRef100_Q9ULH4
UniRef90:
UniRef90_Q9ULH4
UniRef50:
UniRef50_Q80TG9
UniGene:
Hs.250015
CCDS:
CCDS34443.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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