| Monarch Ortholog Phenotypes
|
|
Human (17 sources):
Abnormality of eye movement,
Ataxia,
Chorea,
Craniofacial dystonia,
Dysarthria,
Dyskinesia,
Dysphagia,
Dystonia,
Gait disturbance,
Hyperreflexia,
[+]
|
Mouse (24 sources):
abnormal embryo development,
abnormal heart size,
abnormal heartbeat,
abnormal mitochondrial physiology,
abnormal placenta development,
abnormal placenta fetal blood space morphology,
abnormal placenta intervillous maternal lacunae morphology,
abnormal placenta labyrinth morphology,
abnormal placenta morphology,
abnormal spongiotrophoblast layer morphology,
abnormal trophoblast giant cell morphology,
abnormal visceral yolk sac morphology,
abnormal vitelline vasculature morphology,
absent heartbeat,
decreased embryo size,
decreased spongiotrophoblast cell number,
decreased trophoblast giant cell number,
delayed heart development,
disorganized placental labyrinth,
embryonic growth retardation,
embryonic lethality during organogenesis, complete penetrance,
embryonic lethality, complete penetrance,
pale yolk sac,
prenatal lethality, complete penetrance
[+]
|
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.