KCNMB2 (Q18035155)

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protein-coding gene in the species Homo sapiens

potassium calcium-activated channel subfamily M regulatory beta subunit 2

Language	Label	Description	Also known as
English	KCNMB2	protein-coding gene in the species Homo sapiens	potassium calcium-activated channel subfamily M regulatory beta subunit 2

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000197584

Protein KCNMB2 PDB 1jo6.png
525 × 294; 37 KB

0 references

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

Potassium calcium-activated channel subfamily M regulatory beta subunit 2

1 reference

6 July 2017

UniProt protein ID

genetic association

amyotrophic lateral sclerosis

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=10242

http://www.genome.gov/gwastudies/index.cfm?gene=KCNMB2

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations

25 May 2020

bipolar disorder

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_3312&ncbiId=10242

http://www.genome.gov/gwastudies/index.cfm?gene=KCNMB2

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_5419&ncbiId=10242

http://www.genome.gov/gwastudies/index.cfm?gene=KCNMB2

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder

25 May 2020

lymphoblastic leukemia

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1037&ncbiId=10242

http://www.genome.gov/gwastudies/index.cfm?gene=KCNMB2

Germline genomic variants associated with childhood acute lymphoblastic leukemia

25 May 2020

human chromosome 3

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

178272932

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

177990720

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

178844429

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

178562217

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

cytogenetic location

3q26.32

1 reference

15 May 2022

4257

1 reference

15 May 2022

Gene Atlas image

PBB GE KCNMB2 221097 s at fs.png
732 × 530; 11 KB

0 references

1 reference

HomoloGene build68

4257

1 reference

HomoloGene build68

4257

1 reference

HomoloGene build68

4257

si:ch211-247n2.1

1 reference

HomoloGene build68

4257

islet of Langerhans

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

right uterine tube

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

bronchial epithelial cell

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

caput epididymis

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

corpus epididymis

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

cingulate gyrus

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

prefrontal cortex

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

Brodmann area 23

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

Brodmann area 9

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

smooth muscle tissue

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000197584

http://identifiers.org/ncbigene/10242

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

Ensembl gene ID

ENSG00000197584

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

Ensembl transcript ID

ENST00000358316

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000420517

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000422927

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000432997

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000436247

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000437510

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000452583

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000455865

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

ENST00000470361

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000197584

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)

cywiki KCNMB2
enwiki KCNMB2
ukwiki KCNMB2

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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