tspan7 Phenotypes

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Phenotypes

XB-GENEPAGE-941773

Gene Symbol: tspan7 Gene Name: tetraspanin 7

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (38 sources): 2-3 toe syndactyly, Attention deficit hyperactivity disorder, Autistic behavior, Babinski sign, Bilateral tonic-clonic seizure, Broad nasal tip, Clinodactyly of the 2nd toe, Delayed eruption of teeth, Delayed speech and language development, Depressed nasal bridge, Downslanted palpebral fissures, Drooling, Facial palsy, Generalized non-motor (absence) seizure, Global developmental delay, Intellectual disability, mild, Intellectual disability, moderate, Intellectual disability, profound, Intellectual disability, severe, Long palpebral fissure, Long philtrum, Macrocephaly, Meckel diverticulum, Midface retrusion, Mild neurosensory hearing impairment, Moderate sensorineural hearing impairment, Obesity, Periorbital fullness, Pes planus, Poor speech, Pyloric stenosis, Seizure, Shortening of all distal phalanges of the fingers, Small for gestational age, Thick lower lip vermilion, Thin upper lip vermilion, Urinary incontinence, Widened subarachnoid space [+]
Mouse (9 sources): abnormal action potential, abnormal hippocampus neuron morphology, abnormal miniature excitatory postsynaptic currents, abnormal response to novel object, abnormal spatial working memory, decreased dendritic spine density, impaired contextual conditioning behavior, impaired spatial learning, reduced long term potentiation
View all ortholog results at Monarch