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Symbol
Name
ID
Hnrnph2
heterogeneous nuclear ribonucleoprotein H2
MGI:1201779
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Secondary microcephaly
Drooling
Cerebellar hypoplasia
Ataxia
Absent speech
Anxiety
Conspicuously happy disposition
Autistic behavior
Aggressive behavior
Compulsive behaviors
Attention deficit hyperactivity disorder
Motor stereotypy
Recurrent hand flapping
Self-injurious behavior
Intellectual disability
Gait disturbance
Developmental regression
Global developmental delay
Seizure
Disease(s) Associated with HNRNPH2
syndromic X-linked intellectual developmental disorder bain type

Mouse Phenotypes
nervous system phenotype
audiogenic seizures
hydrocephaly
abnormal cerebral aqueduct morphology
abnormal dendrite arborization pattern
abnormal autonomic nervous system physiology
abnormal brain wave pattern
Availability Mouse Genotype
Hnrnph2em2Jpat/Hnrnph2em2Jpat
Hnrnph2em1Jpat/Hnrnph2+
Hnrnph2em2Jpat/Hnrnph2+
Hnrnph2em1Jpat/Y
Hnrnph2em2Jpat/Y
Hnrnph2em3Jpat/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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last database update
05/14/2024
MGI 6.23
The Jackson Laboratory