| Monarch Ortholog Phenotypes
|
Human (23 sources):
Areflexia,
Camptodactyly of finger,
Cleft palate,
Decreased fetal movement,
Diaphragmatic paralysis,
Diaphragmatic weakness,
Difficulty running,
Dysphagia,
Facial palsy,
Failure to thrive,
High palate,
Hyporeflexia,
Motor delay,
Nasal speech,
Neonatal hypotonia,
Pectus excavatum,
Poor head control,
Respiratory distress,
Respiratory insufficiency,
Restrictive ventilatory defect,
Scoliosis,
Seizure,
Talipes equinovarus
[+]
|
|
Mouse (4 sources):
abnormal amacrine cell morphology,
abnormal astrocyte physiology,
abnormal retina horizontal cell morphology,
increased hindbrain apoptosis
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View all ortholog results at Monarch
|
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.