LINGO2 (Q18052365)

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protein-coding gene in the species Homo sapiens

LERN3
LRRN6C
leucine rich repeat and Ig domain containing 2

Language	Label	Description	Also known as
English	LINGO2	protein-coding gene in the species Homo sapiens	LERN3 LRRN6C leucine rich repeat and Ig domain containing 2

Statements

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000174482

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

Leucine rich repeat and Ig domain containing 2

1 reference

6 July 2017

UniProt protein ID

genetic association

type 2 diabetes

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9352&ncbiId=158038

http://www.genome.gov/gwastudies/index.cfm?gene=LINGO2

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

25 May 2020

endometrial cancer

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1380&ncbiId=158038

http://www.genome.gov/gwastudies/index.cfm?gene=LINGO2

Genome-wide association study of endometrial cancer in E2C2

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9970&ncbiId=158038

http://www.genome.gov/gwastudies/index.cfm?gene=LINGO2

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

25 May 2020

human chromosome 9

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

27948078

human chromosome 9

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

27948076

human chromosome 9

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

28670286

human chromosome 9

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

28670283

human chromosome 9

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

cytogenetic location

9p21.2-p21.1

1 reference

9 January 2022

17621

1 reference

9 January 2022

1 reference

HomoloGene build68

17621

1 reference

HomoloGene build68

17621

si:ch211-170a17.1

1 reference

HomoloGene build68

17621

secondary oocyte

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

endothelial cell

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

middle temporal gyrus

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

Brodmann area 23

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

entorhinal cortex

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

islet of Langerhans

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

Brodmann area 46

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

cerebellar vermis

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000174482

http://identifiers.org/ncbigene/158038

1 reference

Identifiers.org

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

Identifiers

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

Ensembl gene ID

ENSG00000174482

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

Ensembl transcript ID

ENST00000613945

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

ENST00000308675

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

ENST00000379992

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

ENST00000493941

1 reference

ensembl Release 105

Ensembl gene ID

ENSG00000174482

0 references

HGNC gene symbol

1 reference

9 January 2022

1 reference

9 January 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(6 entries)

arwiki LINGO2
arzwiki LINGO2
bswiki LINGO2
enwiki LINGO2
ttwiki LINGO2
ukwiki LINGO2

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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