bicd2l Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (218)

Interactants (1)

XB-GENEPAGE-995876

Gene Symbol: bicd2l Gene Name: BICD cargo adaptor 2 like

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: bicd2l assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (50 sources): Abnormal foot morphology, Abnormal pinna morphology, Abnormality of the Achilles tendon, Achilles tendon contracture, Areflexia, Arthrogryposis multiplex congenita, Axial muscle weakness, Cerebellar hypoplasia, Cerebral cortical atrophy, Congenital foot contraction deformities, Congenital hip dislocation, Decreased fetal movement, Difficulty running, Difficulty walking, Distal lower limb amyotrophy, Distal muscle weakness, Fasciculations, Feeding difficulties, Flexion contracture, Gowers sign, Hand clenching, Hand muscle weakness, Hip contracture, Hip dysplasia, Hyperlordosis, Hyperreflexia, Hypoplasia of the corpus callosum, Hyporeflexia, Knee flexion contracture, Kyphosis, Macrocephaly, Micrognathia, Midface retrusion, Motor delay, Overlapping fingers, Polymicrogyria, Proximal muscle weakness, Respiratory insufficiency, Respiratory insufficiency due to muscle weakness, Scapular winging, Scoliosis, Severe muscular hypotonia, Shoulder girdle muscle weakness, Skeletal muscle atrophy, Spasticity, Spinal muscular atrophy, Talipes equinovarus, Ventriculomegaly, Waddling gait, obsolete Toe walking [+]
Mouse (29 sources): abnormal Purkinje cell dendrite morphology, abnormal brain ependyma morphology, abnormal cerebellar Golgi cell morphology, abnormal cerebellar Purkinje cell layer, abnormal cerebellar granule cell migration, abnormal cerebellar layer morphology, abnormal cerebellar molecular layer, abnormal cerebellum white matter morphology, abnormal extracellular matrix morphology, abnormal hippocampus layer morphology, abnormal hippocampus pyramidal cell layer, abnormal septum pellucidum morphology, abnormal stratification in cerebral cortex, absent cerebellar granule layer, decreased brain external capsule size, decreased corpus callosum size, domed cranium, enlarged lateral ventricles, forebrain atrophy, hippocampus atrophy, limb grasping, long stride length, nervous system phenotype, no abnormal phenotype detected, postnatal lethality, incomplete penetrance, premature death, small cerebellum, striatum atrophy, thin cerebral cortex [+]
View all ortholog results at Monarch