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Symbol
Name
ID

Zfp335
zinc finger protein 335
MGI:2682313

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Primary microcephaly	Spasticity	Gliosis	Delayed CNS myelination	Simplified gyral pattern	Agenesis of corpus callosum	Reduced cerebral white matter volume	Cerebral atrophy	Cerebellar hemisphere hypoplasia	Cerebellar atrophy	Severe global developmental delay
Disease(s) Associated with ZNF335
primary autosomal recessive microcephaly 10

Mouse Phenotypes		decreased brain size	loss of cortex neurons	thin cerebral cortex
Availability	Mouse Genotype	decreased brain size	loss of cortex neurons	thin cerebral cortex
	Zfp335^tm1.1Caw/Zfp335^tm1.1Caw Emx1^tm1(cre)Krj/Emx1⁺ (conditional)
	Zfp335^tm1.1Caw/Zfp335⁺ Emx1^tm1(cre)Krj/Emx1⁺ (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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