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Symbol Name ID |
Hnrnph2
heterogeneous nuclear ribonucleoprotein H2 MGI:1201779 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypertelorism |
Hypotelorism |
Exotropia |
| Disease(s) Associated with HNRNPH2 | |||
| syndromic X-linked intellectual developmental disorder bain type |
| Mouse Phenotypes | ocular hypertelorism |
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| Availability | Mouse Genotype | |
| Hnrnph2em1Jpat/Y | ||
| Hnrnph2em2Jpat/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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