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Symbol
Name
ID
Snrpn
small nuclear ribonucleoprotein N
MGI:98347
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties in infancy
Poor suck
Attention deficit hyperactivity disorder
Behavioral abnormality
Polyphagia
Aggressive behavior
Impaired ability to form peer relationships
Impaired use of nonverbal behaviors
Lack of peer relationships
Autism
Restrictive behavior
Impulsivity
Inflexible adherence to routines or rituals
Lack of spontaneous play
Psychosis
Sleep disturbance
Sleep apnea
Nasal speech
Disease(s) Associated with SNRPN
autistic disorder
Prader-Willi syndrome

Mouse Phenotypes
absent gastric milk in neonates
abnormal suckling behavior
weakness
abnormal stationary movement
Availability Mouse Genotype
Snrpntm1Kaj/Snrpn+
Snrpntm2Cbr/Snrpn+
Snrpntm2.1Kaj/Snrpn+
Alpltm1(cre)Nagy/Alpl+  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
05/14/2019
MGI 6.14
The Jackson Laboratory