Phenotypes Associated with This Genotype

Genotype
MGI:2665400

• Allelic Composition: Fmr1^tm1Cgr/Fmr1^tm1Cgr
• Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

behavior/neurological

increased exploration in new environment ( J:19220 )

♀ • mutants exhibit more exploratory behavior than controls, displaying more line crossings in the lit compartment

increased locomotor activity ( J:19220 )

♀ • mutants show significantly more crossings through three infrared beams in an empty cage over 40 min

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
fragile X syndrome		DOID:14261	OMIM:300624	J:19220