PTPRN2 (Q18030950)

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protein-coding gene in the species Homo sapiens

IA-2beta
IAR
ICAAR
PTPRP
R-PTP-N2
protein tyrosine phosphatase, receptor type N2
protein tyrosine phosphatase receptor type N2

Language	Label	Description	Also known as
English	PTPRN2	protein-coding gene in the species Homo sapiens	IA-2beta IAR ICAAR PTPRP R-PTP-N2 protein tyrosine phosphatase, receptor type N2 protein tyrosine phosphatase receptor type N2

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

protein-coding gene

1 reference

NCBI homo sapiens annotation release 107

3 October 2016

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

Protein tyrosine phosphatase receptor type N2

1 reference

16 March 2017

UniProt protein ID

Receptor-type tyrosine-protein phosphatase N2

1 reference

UniProt protein ID

21 March 2016

language of work or name

genetic association

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9970&ncbiId=5799

http://www.genome.gov/gwastudies/index.cfm?gene=PTPRN2

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_11830&ncbiId=5799

http://www.genome.gov/gwastudies/index.cfm?gene=PTPRN2

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

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_5419&ncbiId=5799

http://www.genome.gov/gwastudies/index.cfm?gene=PTPRN2

Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes

25 May 2020

bipolar disorder

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_3312&ncbiId=5799

http://www.genome.gov/gwastudies/index.cfm?gene=PTPRN2

Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes

25 May 2020

human chromosome 7

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

157539056

human chromosome 7

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

157331750

human chromosome 7

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

158380480

human chromosome 7

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

158587823

human chromosome 7

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

cytogenetic location

7q36.3

1 reference

15 May 2022

2134

1 reference

15 May 2022

Gene Atlas image

PBB GE PTPRN2 203029 s at fs.png
732 × 530; 12 KB

0 references

PBB GE PTPRN2 203030 s at fs.png
732 × 530; 11 KB

0 references

PBB GE PTPRN2 211534 x at fs.png
732 × 530; 12 KB

0 references

1 reference

HomoloGene build68

2134

1 reference

HomoloGene build68

2134

1 reference

HomoloGene build68

2134

middle temporal gyrus

1

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

external globus pallidus

2

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

Brodmann area 23

3

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

entorhinal cortex

4

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

orbitofrontal cortex

5

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

6

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

superior frontal gyrus

7

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

Brodmann area 46

8

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

postcentral gyrus

9

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

bronchial epithelial cell

10

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000155093

http://identifiers.org/ncbigene/5799

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

10 April 2022

1 reference

10 April 2022

1 reference

10 April 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000155093

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENSG00000282185

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

Ensembl transcript ID

ENST00000389413

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000389416

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000389418

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000404321

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000409483

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000631503

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000632665

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000633393

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000633583

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

ENST00000648371

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000155093

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(5 entries)

arwiki PTPRN2
arzwiki PTPRN2
enwiki PTPRN2
ttwiki PTPRN2
ukwiki PTPRN2

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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