(Q18043142)

English

LRRC7

protein-coding gene in the species Homo sapiens

DENSIN
leucine rich repeat containing 7

In more languages

default for all languages

No label defined

No description defined

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000033122

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

Leucine rich repeat containing 7

1 reference

6 July 2017

UniProt protein ID

Leucine-rich repeat-containing protein 7

1 reference

UniProt protein ID

20 March 2016

language of work or name

genetic association

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9970&ncbiId=57554

http://www.genome.gov/gwastudies/index.cfm?gene=LRRC7

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

10 April 2020

cleft lip and cleft palate

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_0050567&ncbiId=57554

http://www.genome.gov/gwastudies/index.cfm?gene=LRRC7

Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts

10 April 2020

arterial hypertension

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10763&ncbiId=57554

http://www.genome.gov/gwastudies/index.cfm?gene=LRRC7

Genetic association of short sleep duration with hypertension incidence--a 6-year follow-up in the Korean genome and epidemiology study

10 April 2020

attention deficit hyperactivity disorder

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1094&ncbiId=57554

http://www.genome.gov/gwastudies/index.cfm?gene=LRRC7

Genome-wide association study of the child behavior checklist dysregulation profile

10 April 2020

human chromosome 1

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

70034081

human chromosome 1

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

69567922

human chromosome 1

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

70151945

human chromosome 1

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

70617628

human chromosome 1

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

cytogenetic location

1p31.1

1 reference

15 May 2022

10817

1 reference

15 May 2022

1 reference

HomoloGene build68

10817

1 reference

HomoloGene build68

10817

1 reference

HomoloGene build68

10817

Brodmann area 23

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

primary visual cortex

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

nucleus accumbens

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

middle temporal gyrus

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

Brodmann area 9

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

ganglionic eminence

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

caudate nucleus

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

Brodmann area 46

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

hippocampus proper

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000033122

http://identifiers.org/ncbigene/57554

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

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

Ensembl gene ID

ENSG00000033122

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

Ensembl transcript ID

ENST00000609498

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000310961

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000370958

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000415775

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000441830

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000565615

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000588515

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000607936

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000608470

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000608744

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000608815

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000609072

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000651989

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

ENST00000651217

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000033122

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

Microsoft Academic ID

0 references

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(3 entries)

enwiki LRRC7
ttwiki LRRC7
ukwiki LRRC7

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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