Symbol Name ID |
Sh3pxd2b
SH3 and PX domains 2B MGI:2442062 |
Darker colors indicate more annotations |
Human Phenotypes | Redundant neck skin |
Inguinal hernia |
Umbilical hernia |
Growth delay |
Disease(s) Associated with SH3PXD2B | ||||
Frank-Ter Haar syndrome |
Mouse Phenotypes | decreased body fat mass |
abnormal tooth morphology |
short nasal bone |
short snout |
decreased body weight |
decreased body size |
proportional dwarf |
abnormal postnatal growth |
postnatal growth retardation |
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Availability | Mouse Genotype | |||||||||
Sh3pxd2bGt(GST_1527_E5)Lex/Sh3pxd2bGt(GST_1527_E5)Lex | ||||||||||
Sh3pxd2bnee/Sh3pxd2bnee | ||||||||||
Sh3pxd2btm1.1Arte/Sh3pxd2btm1.1Arte |
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 09/03/2024 MGI 6.24 |
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