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ALS3 amyotrophic lateral sclerosis 3 (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 253, updated on 31-Aug-2024

Summary

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Official Symbol
ALS3provided by HGNC
Official Full Name
amyotrophic lateral sclerosis 3 (autosomal dominant)provided by HGNC
Primary source
MIM:606640
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ALS6

Genomic context

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Location:
18q21

Bibliography

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Related articles in PubMed

  1. A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q. Hand CK, et al. Am J Hum Genet, 2002 Jan. PMID 11706389, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
amyotrophic lateral sclerosis 3 (autosomal dominant)
OMIM: 606640GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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