Symbol Name ID |
Hnrnph2
heterogeneous nuclear ribonucleoprotein H2 MGI:1201779 |
* | 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 | * |
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 |
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