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Symbol
Name
ID
Rai1
retinoic acid induced 1
MGI:103291
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties in infancy
Atypical behavior
Onychotillomania
Hyperactivity
Attention deficit hyperactivity disorder
Motor stereotypy
Self hugging
Head-banging
Self-injurious behavior
Self-mutilation
Hyperacusis
Polyembolokoilamania
Hoarse voice
Disease(s) Associated with RAI1
Smith-Magenis syndrome

Mouse Phenotypes
behavior/neurological phenotype
abnormal associative learning
abnormal contextual conditioning behavior
impaired contextual conditioning behavior
abnormal cued conditioning behavior
impaired cued conditioning behavior
abnormal spatial working memory
increased food intake
polyphagia
increased anxiety-related response
limb grasping
impaired coordination
increased vertical activity
decreased locomotor activity
increased locomotor activity
abnormal circadian behavior
decreased vocalization
seizures
tonic-clonic seizures
Availability Mouse Genotype
Rai1tm1Jrl/Rai1tm1Jrl
Rai1tm1Jrl/Rai1+
Tg(Camk2a-tTA)1Mmay/0
Tg(tetO-Rai1,-EGFP)463Walz/0
Tg(Camk2a-tTA)1Mmay/0
Tg(tetO-Rai1,-EGFP)479Walz/0
Rai1tm2.1Luo/Rai1tm2.1Luo
Tg(Nes-cre)1Kln/?  (conditional)
*
Rai1tm2.1Luo/Rai1tm2.1Luo
Slc17a6tm2(cre)Lowl/?  (conditional)
Gad2tm2(cre)Zjh/?
Rai1tm2.1Luo/Rai1tm2.1Luo  (conditional)
Rai1tm2.1Luo/Rai1tm2.1Luo
Tg(Sim1-cre)1Lowl/?  (conditional)
*
Rai1tm2.1Luo/Rai1tm2.1Luo
Tg(Nr5a1-cre)7Lowl/?  (conditional)
*
Rai1tm2.1Luo/Rai1+
Tg(Nes-cre)1Kln/?  (conditional)
Rai1tm2.1Luo/Rai1+
Slc17a6tm2(cre)Lowl/?  (conditional)
Rai1tm2.2Luo/Rai1+
Tg(Nes-cre)1Kln/?  (conditional)

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory