(Q18037094)

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

Phenocarta

retrieved

25 May 2020

periventricular nodular heterotopia 7; PVNH7

2 references

13 August 2019

20 December 2021

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_b131d46a-069b-4c2e-a290-e7df2519a2df-2021-11-30T170000.000Z

periventricular nodular heterotopia

1 reference

https://platform.opentargets.org/evidence/ENSG00000049759/MONDO_0020341

Open Targets Platform

retrieved

24 August 2023

reference URL

based on heuristic

inferred from an Open Targets association score over 0.7

chromosome

human chromosome 18

genomic assembly

1 reference

1 reference

55711599

1 reference

58044226

1 reference

58401540

1 reference

56068772

Saccharomyces cerevisiae S288c

1 reference

18q21.31

1 reference

9 January 2022

86986

1 reference

9 January 2022

1 reference

86986

1 reference

86986

1 reference

86986

1 reference

86986

Caenorhabditis elegans

1 reference

86986

Drosophila melanogaster

1 reference

86986

1

1 reference

19 April 2022

right lung

2

1 reference

19 April 2022

secondary oocyte

3

1 reference

19 April 2022

body of pancreas

4

1 reference

19 April 2022

upper lobe of left lung

5

1 reference

19 April 2022

rectum

6

1 reference

19 April 2022

kidney

7

1 reference

19 April 2022

prostate

8

1 reference

19 April 2022

body of stomach

9

1 reference

19 April 2022

middle temporal gyrus

10

1 reference

19 April 2022

http://identifiers.org/ncbigene/23327

exact match

1 reference

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers.org

reference URL

Identifiers

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

9 January 2022

1 reference

Ensembl transcript ID

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

1 reference

0 references

1 reference

9 January 2022

1 reference

9 January 2022

Microsoft Academic ID

0 references

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

inferred by common HGNC mappings on source and on Wikidata