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Symbol
Name
ID

Reln
reelin
MGI:103022

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties	Lack of spontaneous play	Impaired ability to form peer relationships	Autism	Inflexible adherence to routines	Motor stereotypy	Restrictive behavior
Disease(s) Associated with RELN	Feeding difficulties	Lack of spontaneous play	Impaired ability to form peer relationships	Autism	Inflexible adherence to routines	Motor stereotypy	Restrictive behavior
autistic disorder
Norman-Roberts syndrome

Mouse Phenotypes

behavior/neurological phenotype

abnormal short-term spatial reference memory

abnormal motor capabilities/coordination/movement

impaired righting response

tremors

abnormal motor coordination/balance

ataxia

impaired balance

impaired coordination

abnormal posture

abnormal gait

decreased locomotor activity

abnormal sexual interaction

abnormal social investigation

Availability

Mouse Genotype

Reln^m1Anu/Reln^m1Anu

Reln^rl-4J/Reln^rl-4J

Reln^rl-5J/Reln^rl-5J

Reln^rl-6J/Reln^rl-6J

Reln^rl-7J/Reln^rl-7J

Reln^rl-8J/Reln^rl-8J

Reln^rl-Alb2/Reln^rl-Alb2

Reln^rl-Alb/Reln^rl-Alb

Reln^rl-od/Reln^rl-od

Reln^rl-tg/Reln^rl-tg

Reln^rl/Reln^rl

*!

!

!

!

!

Reln^tm1.1Mhat/Reln^tm1.1Mhat

*

Reln^rl/Reln⁺

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)
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