MACROD2 (Q18050946)

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protein-coding gene in the species Homo sapiens

C20orf133
MACRO domain containing 2
C2orf133
mono-ADP ribosylhydrolase 2

Language	Label	Description	Also known as
English	MACROD2	protein-coding gene in the species Homo sapiens	C20orf133 MACRO domain containing 2 C2orf133 mono-ADP ribosylhydrolase 2

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000172264

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

Mono-ADP ribosylhydrolase 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=140733

http://www.genome.gov/gwastudies/index.cfm?gene=MACROD2

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

25 May 2020

eating disorder

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_8670&ncbiId=140733

http://www.genome.gov/gwastudies/index.cfm?gene=MACROD2

Genetic variants associated with disordered eating

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9970&ncbiId=140733

http://www.genome.gov/gwastudies/index.cfm?gene=MACROD2

Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population

25 May 2020

fatty liver disease

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9452&ncbiId=140733

http://www.genome.gov/gwastudies/index.cfm?gene=MACROD2

Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease

25 May 2020

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_12849&ncbiId=140733

http://www.genome.gov/gwastudies/index.cfm?gene=MACROD2

A genome-wide scan for common alleles affecting risk for autism

25 May 2020

human chromosome 20

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

13995369

human chromosome 20

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

13976015

human chromosome 20

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

16053197

human chromosome 20

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

16033842

human chromosome 20

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

cytogenetic location

20p12.1

1 reference

15 May 2022

85987

1 reference

15 May 2022

1 reference

HomoloGene build68

85987

1 reference

HomoloGene build68

85987

Caenorhabditis elegans

1 reference

HomoloGene build68

85987

endothelial cell

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

pancreatic epithelial cell

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

lower lobe of lung

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

Brodmann area 23

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

germinal epithelium

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

middle temporal gyrus

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

entorhinal cortex

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

visceral pleura

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

Brodmann area 46

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000172264

http://identifiers.org/ncbigene/140733

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

ENSG00000172264

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

Ensembl transcript ID

ENST00000497992

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000217246

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000378058

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000402914

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000407045

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000462552

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000463861

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000464883

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000477147

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000483997

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000486914

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000490428

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000492055

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000494602

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000642719

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

ENST00000684519

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000172264

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 MACROD2
ukwiki MACROD2

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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