ascc1 activating signal cointegrator 1 complex subunit 1
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.
|Computed annotations: ascc1 assayed (2 sources)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (27 sources):
Abnormal cortical gyration,
Arthrogryposis multiplex congenita,
Decreased fetal movement,
Gastroesophageal reflux, Generalized hypotonia, Global developmental delay, Increased variability in muscle fiber diameter, Multiple prenatal fractures, Muscle weakness, Neonatal respiratory distress, Patent ductus arteriosus, Patent foramen ovale, Peripheral axonal neuropathy, Polyhydramnios, Premature birth, Pulmonary hypoplasia, Respiratory insufficiency, Severe muscular hypotonia, Skeletal muscle atrophy, Spinal muscular atrophy[+]
|Mouse (3 sources): abnormal body wall morphology, abnormal embryo size, preweaning lethality, incomplete penetrance|
View all ortholog results at Monarch