cog7 Phenotypes

Phenotypes

XB-GENEPAGE-970836

Gene Symbol: cog7 Gene Name: component of oligomeric golgi complex 7

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (54 sources): Abnormal facial shape, Abnormal heart morphology, Abnormal pinna morphology, Abnormality of immune system physiology, Abnormality of the skeletal system, Adducted thumb, Cerebellar atrophy, Cerebral atrophy, Congestive heart failure, Decreased liver function, Delayed myelination, Elevated circulating creatine kinase concentration, Elevated circulating hepatic transaminase concentration, Failure to thrive, Feeding difficulties, Flat forehead, Gastroesophageal reflux, Generalized hypotonia, Growth delay, Hearing impairment, Hepatomegaly, Hydronephrosis, Hypertrichosis, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoplasia of the corpus callosum, Hyporeflexia, Hypotonia, Intrauterine growth retardation, Inverted nipples, Jaundice, Low anterior hairline, Low-set ears, Micrognathia, Narrow forehead, Narrow mouth, Neurogenic bladder, Overlapping fingers, Profound global developmental delay, Progressive microcephaly, Protruding tongue, Respiratory insufficiency, Retrognathia, Seizure, Short neck, Short nose, Short palpebral fissure, Short stature, Skeletal muscle atrophy, Smooth philtrum, Splenomegaly, Thick vermilion border, Upslanted palpebral fissure, Wide nose [+]
Mouse (2 sources): embryonic lethality prior to organogenesis, preweaning lethality, complete penetrance
View all ortholog results at Monarch