amyotrophic lateral sclerosis type 2 Disease Ontology Browser

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Disease Ontology Browser

amyotrophic lateral sclerosis type 2 (DOID:0060194)
Alliance: disease page
Synonyms: ALS2; amyotrophic lateral sclerosis 2; amyotrophic lateral sclerosis 2, juvenile
Alt IDs: OMIM:205100, ICD10CM:G12.2
Definition: An amyotrophic lateral sclerosis that has_material_basis_in mutation in the alsin gene on chromosome 2.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/10/2024 MGI 6.24

Allelic Composition	Genetic Background	Reference	Phenotypes
Als2tm1Cai/Als2tm1Cai	involves: 129X1/SvJ * C57BL/6J	J:100336	View
Als2tm1Jei/Als2tm1Jei	involves: 129P2/OlaHsd * C57BL/6J	J:104446	View
Als2tm1Garo/Als2tm1Garo	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	J:138147	View