Symbol
Name
ID

B4gat1
beta-1,4-glucuronyltransferase 1
MGI:1919680

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Dandy-Walker malformation

Occipital encephalocele

Spasticity

Hypoplasia of the brainstem

Hydrocephalus

Communicating hydrocephalus

Ventriculomegaly

Type II lissencephaly

Cortical dysplasia

Abnormal cerebral white matter morphology

Agenesis of corpus callosum

Absent septum pellucidum

Anencephaly

Agenesis of cerebellar vermis

Cerebellar hypoplasia

Cerebellar hemisphere hypoplasia

Hydromyelia

Gray matter heterotopia

Global developmental delay

Seizure

Disease(s) Associated with B4GAT1

congenital muscular dystrophy-dystroglycanopathy type A13

Mouse Phenotypes		abnormal axon fasciculation	abnormal axon guidance	radial glial endfoot detachment	abnormal neuronal migration	hydrocephaly	abnormal nervous system tract morphology	abnormal spinal cord ventral commissure morphology	ectopic neuron	abnormal spinal cord dorsal column morphology
Availability	Mouse Genotype	abnormal axon fasciculation	abnormal axon guidance	radial glial endfoot detachment	abnormal neuronal migration	hydrocephaly	abnormal nervous system tract morphology	abnormal spinal cord ventral commissure morphology	ectopic neuron	abnormal spinal cord dorsal column morphology
	B4gat1^m1Ddg/B4gat1^m1Ddg
	B4gat1^m1Ddg/B4gat1^{tm1(KOMP)Vlcg}

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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