CNTN5 (Q18040744)

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protein-coding gene in the species Homo sapiens

HNB-2s
NB-2
contactin 5

Language	Label	Description	Also known as
English	CNTN5	protein-coding gene in the species Homo sapiens	HNB-2s NB-2 contactin 5

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000149972

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

1 reference

6 July 2017

UniProt protein ID

genetic association

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11830&ncbiId=53942

http://www.genome.gov/gwastudies/index.cfm?gene=CNTN5

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population

25 May 2020

determination method or standard

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_8736&ncbiId=53942

http://www.genome.gov/gwastudies/index.cfm?gene=CNTN5

Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients

25 May 2020

human chromosome 11

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

98891683

human chromosome 11

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

99020949

human chromosome 11

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

100358885

human chromosome 11

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

100229616

human chromosome 11

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

cytogenetic location

11q22.1

1 reference

15 May 2022

28447

1 reference

15 May 2022

2 references

HomoloGene build68

28447

Orthologous MAtrix

https://omabrowser.org/oma/vps/O94779/

2 references

HomoloGene build68

28447

Orthologous MAtrix

https://omabrowser.org/oma/vps/O94779/

2 references

HomoloGene build68

28447

Orthologous MAtrix

https://omabrowser.org/oma/vps/O94779/

Drosophila melanogaster

1 reference

Orthologous MAtrix

https://omabrowser.org/oma/vps/O94779/

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

islet of Langerhans

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

primary visual cortex

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

prefrontal cortex

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

Brodmann area 23

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

middle temporal gyrus

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

cingulate gyrus

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

anterior cingulate cortex

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

stromal cell of endometrium

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000149972

http://identifiers.org/ncbigene/53942

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

10 April 2022

1 reference

10 April 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000149972

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

Ensembl transcript ID

ENST00000279463

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000418526

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000524560

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000524871

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000525047

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000525236

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000527185

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000527682

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000528682

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000528727

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

ENST00000530458

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000149972

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 CNTN5
ukwiki CNTN5

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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