Symbol
Name
ID

Hnrnph2
heterogeneous nuclear ribonucleoprotein H2
MGI:1201779

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Drooling	Feeding difficulties	Conspicuously happy disposition	Autistic behavior	Aggressive behavior	Compulsive behaviors	Attention deficit hyperactivity disorder	Motor stereotypy	Recurrent hand flapping	Self-injurious behavior
Disease(s) Associated with HNRNPH2
syndromic X-linked intellectual developmental disorder bain type

Mouse Phenotypes

behavior/neurological phenotype

abnormal cognition

abnormal habituation to a new environment

impaired spatial learning

abnormal spatial reference memory

abnormal emotion/affect behavior

increased anxiety-related response

increased thigmotaxis

abnormal motor capabilities/coordination/movement

impaired balance

impaired coordination

decreased grip strength

short stride length

decreased locomotor activity

decreased stereotypic behavior

impaired social recognition

abnormal vocalization

audiogenic seizures

Availability

Mouse Genotype

Hnrnph2^em1(IMPC)J/Hnrnph2^em1(IMPC)J

Hnrnph2^em2Jpat/Hnrnph2^em2Jpat

Hnrnph2^em1Jpat/Hnrnph2⁺

Hnrnph2^em1(IMPC)J/Y

Hnrnph2^em1Jpat/Y

Hnrnph2^em2Jpat/Y

Hnrnph2^em3Jpat/Y

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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