b4gat1 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (100)

Interactants (43)

XB-GENEPAGE-1007366

Gene Symbol: b4gat1 Gene Name: beta-1,4-glucuronyltransferase 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (68 sources): Abnormal aldolase level, Abnormal cerebellar vermis morphology, Abnormal circulating creatine kinase concentration, Abnormal circulating lactate dehydrogenase concentration, Abnormal cortical gyration, Abnormality of neuronal migration, Abnormality of the optic nerve, Absent septum pellucidum, Agenesis of corpus callosum, Anencephaly, Anophthalmia, Aplasia/Hypoplasia involving the skeletal musculature, Areflexia, Bifid uvula, Blindness, Cataract, Cerebellar hypoplasia, Chorioretinal dysplasia, Cleft palate, Corneal opacity, Cortical dysplasia, Cryptorchidism, Dandy-Walker malformation, Decreased testicular size, Elevated circulating creatine kinase concentration, Glaucoma, Global developmental delay, Gray matter heterotopia, Hydrocephalus, Hydronephrosis, Hypoplasia of penis, Hypoplasia of the brainstem, Hyporeflexia, Hypotonia, Intellectual disability, Iris coloboma, Lissencephaly, Low-set ears, Macrocephaly, Metatarsus valgus, Microcephaly, Microcornea, Micropenis, Microphthalmia, Muscle weakness, Muscular dystrophy, Occipital encephalocele, Opacification of the corneal stroma, Optic atrophy, Optic nerve dysplasia, Pachygyria, Polymicrogyria, Posteriorly rotated ears, Protruding ear, Renal cyst, Renal dysplasia, Retinal detachment, Retinal dysplasia, Retinal dystrophy, Seizure, Severe muscular hypotonia, Skeletal muscle atrophy, Spasticity, Specific learning disability, Submucous cleft hard palate, Type II lissencephaly, Ventriculomegaly, obsolete Macrogyria [+]
Mouse (24 sources): abnormal anxiety-related response, abnormal axon fasciculation, abnormal axon guidance, abnormal basement membrane morphology, abnormal embryo size, abnormal locomotor activation, abnormal lymph node cell ratio, abnormal nervous system tract morphology, abnormal spinal cord dorsal column morphology, abnormal spinal cord ventral commissure morphology, decreased circulating alanine transaminase level, decreased eosinophil cell number, decreased thigmotaxis, ectopic neuron, embryonic lethality during organogenesis, complete penetrance, embryonic lethality prior to organogenesis, embryonic lethality prior to tooth bud stage, hunched posture, immune system phenotype, impaired leukocyte tethering or rolling, limb grasping, perinatal lethality, incomplete penetrance, preweaning lethality, complete penetrance, radial glial endfoot detachment [+]
View all ortholog results at Monarch