(Q18029240)

English

MOBP

protein-coding gene in the species Homo sapiens

myelin-associated oligodendrocyte basic protein
myelin associated oligodendrocyte basic protein

In more languages

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000168314

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

Myelin associated oligodendrocyte basic protein

1 reference

6 July 2017

UniProt protein ID

Myelin-associated oligodendrocyte basic protein

1 reference

UniProt protein ID

21 March 2016

language of work or name

Myelin-associated oligodendrocyte basic protein, isoform CRA_b

1 reference

UniProt protein ID

20 March 2016

language of work or name

genetic association

Alzheimer's disease

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_10652&ncbiId=4336

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

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

25 May 2020

progressive supranuclear palsy

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_678&ncbiId=4336

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

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

25 May 2020

attention deficit hyperactivity disorder

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_1094&ncbiId=4336

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

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

25 May 2020

human chromosome 3

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

39467198

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

39508689

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

39529479

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

39570970

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

cytogenetic location

3p22.1

1 reference

15 May 2022

32040

1 reference

15 May 2022

1 reference

HomoloGene build68

32040

1 reference

HomoloGene build68

32040

1

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

2

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

corpus callosum

3

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

4

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

inferior ganglion of vagus nerve

5

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

subthalamic nucleus

6

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

superior vestibular nucleus

7

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

pars reticulata

8

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

internal globus pallidus

9

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

10

1 reference

7 June 2024

https://www.bgee.org/gene/ENSG00000168314

http://identifiers.org/ncbigene/4336

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

Ensembl gene ID

ENSG00000168314

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

Ensembl transcript ID

ENST00000311042

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000383754

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000415443

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000420739

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000424090

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000428261

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000436143

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000441980

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000442631

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000447324

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000451925

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000452959

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000479860

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000682069

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

ENST00000684792

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000168314

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 MOBP
ukwiki MOBP

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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