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 | Short stature |
Failure to thrive |
Disease(s) Associated with HNRNPH2 | ||
syndromic X-linked intellectual developmental disorder bain type |
Mouse Phenotypes | short snout |
growth/size/body region phenotype |
decreased body weight |
decreased body size |
|
Availability | Mouse Genotype | ||||
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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