Sgh
Chemically induced Allele Detail

Summary

• Symbol: Sgh
• Name: sluggish
• MGI ID: MGI:2679588
• Synonyms: PLAY 14
• Gene: Sgh Location: unknown Genetic Position: Chr4, Syntenic
• Alliance: Sgh page

Mutation origin

• Strain of Origin: BALB/cOlaHsd

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Undefined
• Mutation details: This phenotypic mutation was identified in an ENU mutagenesis screen at the MRC Mammalian Genetics Unit, Harwell, UK.
• Inheritance: Dominant

Phenotypes

Key:

hm	homozygous	ht	heterozygous	tg	involves transgenes	√	phenotype observed
cn	conditional genotype	cx	complex: > 1 genome feature	ot	other: hemizygous, indeterminate,...	N	normal phenotype

Genotype/
Background:

	Allelic Composition	Genetic Background	Cell Line(s)
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ht1	Sgh/Sgh^+	involves: BALB/cOlaHsd * C3H/HeH

Phenotypes:

Affected Systems	ht1
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behavior/neurological	√
decreased locomotor activity	√

View phenotypes and curated references for all genotypes (concatenated display).

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any Sgh Mutation: 2 strains or lines available

References

• Original: J:86361 Bacon Y, et al., Screening for novel ENU-induced rhythm, entrainment and activity mutants. MGI Direct Data Submission. 2003
• All: 2 reference(s)