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Symbol
Name
ID

Cul4b
cullin 4B
MGI:1919834

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Short neck	Inguinal hernia	Delayed puberty	Short stature	Cachexia	Obesity	Abdominal obesity
Disease(s) Associated with CUL4B
syndromic X-linked intellectual disability Cabezas type

Mouse Phenotypes		embryonic growth retardation	decreased embryo size	decreased body weight	decreased body size	postnatal growth retardation	decreased fetal size	fetal growth retardation
Availability	Mouse Genotype	embryonic growth retardation	decreased embryo size	decreased body weight	decreased body size	postnatal growth retardation	decreased fetal size	fetal growth retardation
	Cul4b^tm1.1Yxg/Cul4b⁺
	Cul4b^tm1.1Yxg/Y
	Cul4b^tm1.1Pz/Y Tg(CAG-cre)13Miya/0 (conditional)

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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