LRFN2 (Q18043088)

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protein-coding gene in the species Homo sapiens

FIGLER2
KIAA1246
SALM1
leucine rich repeat and fibronectin type III domain containing 2

Language	Label	Description	Also known as
English	LRFN2	protein-coding gene in the species Homo sapiens	FIGLER2 KIAA1246 SALM1 leucine rich repeat and fibronectin type III domain containing 2

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000156564

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

Leucine rich repeat and fibronectin type III domain containing 2

1 reference

6 July 2017

UniProt protein ID

genetic association

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9970&ncbiId=57497

http://www.genome.gov/gwastudies/index.cfm?gene=LRFN2

Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10534&ncbiId=57497

http://www.genome.gov/gwastudies/index.cfm?gene=LRFN2

Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1324&ncbiId=57497

http://www.genome.gov/gwastudies/index.cfm?gene=LRFN2

Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese

25 May 2020

squamous cell carcinoma

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1749&ncbiId=57497

http://www.genome.gov/gwastudies/index.cfm?gene=LRFN2

Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese

25 May 2020

human chromosome 6

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

40359325

human chromosome 6

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

40391591

human chromosome 6

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

40555204

human chromosome 6

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

40587364

human chromosome 6

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

cytogenetic location

6p21.2-p21.1

1 reference

15 May 2022

19182

1 reference

15 May 2022

1 reference

HomoloGene build68

19182

1 reference

HomoloGene build68

19182

1 reference

HomoloGene build68

19182

prefrontal cortex

1

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

Brodmann area 9

2

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

islet of Langerhans

3

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

4

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

5

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

hippocampus proper

6

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

superior frontal gyrus

7

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

ganglionic eminence

8

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

postcentral gyrus

9

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

substantia nigra

10

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000156564

http://identifiers.org/ncbigene/57497

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000156564

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

Ensembl transcript ID

ENST00000338305

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000156564

Google Knowledge Graph ID

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(2 entries)

ttwiki LRFN2
ukwiki LRFN2

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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