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Symbol
Name
ID

Sh3pxd2b
SH3 and PX domains 2B
MGI:2442062

Phenotype annotations related to growth/size/body

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
Availability	Mouse Genotype	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
	Sh3pxd2b^{Gt(GST_1527_E5)Lex}/Sh3pxd2b^{Gt(GST_1527_E5)Lex}
	Sh3pxd2b^nee/Sh3pxd2b^nee
	Sh3pxd2b^tm1.1Arte/Sh3pxd2b^tm1.1Arte

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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