slc6a9 Phenotypes

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Phenotypes

Gene Literature (34)

Nucleotides (88)

Interactants (42)

XB-GENEPAGE-948181

Gene Symbol: slc6a9 Gene Name: solute carrier family 6 member 9

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (33 sources): Anteverted nares, Apnea, Arthrogryposis multiplex congenita, Axial hypotonia, Clonus, Depressed nasal bridge, Dolichocephaly, Dysphagia, Elbow flexion contracture, Encephalopathy, Exaggerated startle response, Fetal distress, Flexion contracture, Genu recurvatum, Global developmental delay, Hand clenching, Hip contracture, Hip dislocation, Hypoplasia of the corpus callosum, Long eyelashes, Low-set ears, Microcephaly, Myopathic facies, Optic atrophy, Overlapping toe, Ptosis, Respiratory insufficiency, Retrognathia, Spasticity, Talipes equinovarus, Trigonocephaly, Ventriculomegaly, obsolete Joint laxity [+]
Mouse (26 sources): abnormal NMDA-mediated synaptic currents, abnormal active avoidance behavior, abnormal breathing pattern, abnormal conditioned taste aversion behavior, abnormal cued conditioning behavior, abnormal inhibitory postsynaptic currents, abnormal latent inhibition of conditioning behavior, abnormal limb posture, abnormal motor capabilities/coordination/movement, abnormal neuron physiology, abnormal sensorimotor gating, abnormal spatial learning, abnormal suckling behavior, absent gastric milk in neonates, behavior/neurological phenotype, decreased pulmonary respiratory rate, enhanced NMDA-mediated synaptic currents, hyporesponsive to tactile stimuli, impaired behavioral response to addictive substance, muscle phenotype, neonatal lethality, complete penetrance, nervous system phenotype, no abnormal phenotype detected, postnatal lethality, incomplete penetrance, prenatal lethality, complete penetrance, preweaning lethality, complete penetrance [+]
View all ortholog results at Monarch