NKAIN2 (Q18052271)

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protein-coding gene in the species Homo sapiens

FAM77B
NKAIP2
TCBA
TCBA1
Na+/K+ transporting ATPase interacting 2
sodium/potassium transporting ATPase interacting 2

Language	Label	Description	Also known as
English	NKAIN2	protein-coding gene in the species Homo sapiens	FAM77B NKAIP2 TCBA TCBA1 Na+/K+ transporting ATPase interacting 2 sodium/potassium transporting ATPase interacting 2

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000188580

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

Sodium/potassium transporting ATPase interacting 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_824&ncbiId=154215

http://www.genome.gov/gwastudies/index.cfm?gene=NKAIN2

Genome-wide association study of chronic periodontitis in a general German population

25 May 2020

Alzheimer's disease

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10652&ncbiId=154215

http://www.genome.gov/gwastudies/index.cfm?gene=NKAIN2

Genome-wide association study of the rate of cognitive decline in Alzheimer's disease

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_5419&ncbiId=154215

http://www.genome.gov/gwastudies/index.cfm?gene=NKAIN2

A comprehensive family-based replication study of schizophrenia genes

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10608&ncbiId=154215

http://www.genome.gov/gwastudies/index.cfm?gene=NKAIN2

Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus

25 May 2020

human chromosome 6

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

124125286

human chromosome 6

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

123803865

human chromosome 6

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

125146803

human chromosome 6

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

124825640

human chromosome 6

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

cytogenetic location

6q22.31

1 reference

15 May 2022

65073

1 reference

15 May 2022

1 reference

HomoloGene build68

65073

1 reference

HomoloGene build68

65073

1 reference

HomoloGene build68

65073

corpus callosum

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

inferior ganglion of vagus nerve

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

Brodmann area 46

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

medulla oblongata

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

subthalamic nucleus

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

superior vestibular nucleus

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

hippocampus proper

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

substantia nigra

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

prefrontal cortex

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000188580

http://identifiers.org/ncbigene/154215

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

10 April 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000188580

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

Ensembl transcript ID

ENST00000368416

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

ENST00000368417

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

ENST00000476571

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

ENST00000545433

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

ENST00000546092

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

ENST00000640160

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000188580

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 NKAIN2
ukwiki NKAIN2

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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