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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

Nasogastric tube feeding in infancy

Poor suck

Tube feeding

Atypical behavior

Autistic behavior

Autism

Polyphagia

Attention deficit hyperactivity disorder

Self-injurious behavior

Weak cry

Hypernasal speech

Disease(s) Associated with SNRPN

Prader-Willi syndrome

Mouse Phenotypes		absent gastric milk in neonates	abnormal suckling behavior	weakness	abnormal stationary movement
Availability	Mouse Genotype	absent gastric milk in neonates	abnormal suckling behavior	weakness	abnormal stationary movement
	Snrpn^tm1Rsnk/Snrpn⁺
	Snrpn^tm2Cbr/Snrpn⁺
	Snrpn^tm2.1Kaj/Snrpn⁺ Alpl^tm1(cre)Nagy/Alpl⁺ (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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