dync1i2 Phenotypes

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Phenotypes

Gene Literature (4)

Nucleotides (346)

Interactants (352)

XB-GENEPAGE-960811

Gene Symbol: dync1i2 Gene Name: dynein, cytoplasmic 1, intermediate chain 2

Anatomical Phenotypes Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormal bending of tail (1 source), abnormal heart morphology (1 source), abnormal tail morphology (1 source), abnormal trunk morphology (1 source), decreased length of anterior-posterior axis (1 source), decreased size of the head (1 source), wholly ventralized embryo (1 source)

Experiments (Reagents) These are short form descriptions of experiments using reagents targeting the gene of interest.
Xtr Wt + dync1i2 MO (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (29 sources): Absent septum pellucidum, Agenesis of corpus callosum, Aggressive behavior, Anteverted nares, Attention deficit hyperactivity disorder, Bulbous nose, Cerebral atrophy, Delayed ability to walk, Delayed speech and language development, Dysarthria, Generalized hypotonia, Global developmental delay, Hyperreflexia, Hypoplasia of the brainstem, Hypoplasia of the corpus callosum, Inability to walk, Intellectual disability, severe, Microcephaly, Motor delay, Nasal speech, Prominent nose, Proptosis, Seizure, Severe global developmental delay, Short stature, Simplified gyral pattern, Sloping forehead, Spasticity, Upslanted palpebral fissure [+]
Mouse (1 source): abnormal locomotor behavior
View all ortholog results at Monarch