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Symbol
Name
ID
Ercc6
excision repair cross-complementing rodent repair deficiency, complementation group 6
MGI:1100494
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Splenomegaly
Hepatomegaly
Delayed puberty
Severe short stature
Failure to thrive
Severe failure to thrive
Small for gestational age
Cachexia
Growth delay
Intrauterine growth retardation
Postnatal growth retardation
Disease(s) Associated with ERCC6
cerebrooculofacioskeletal syndrome 1
Cockayne syndrome
Cockayne syndrome B
De Sanctis-Cacchione syndrome

Mouse Phenotypes
decreased body weight
postnatal growth retardation
Availability Mouse Genotype
Ercc6tm1Gvh/Ercc6tm1Gvh

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
05/14/2024
MGI 6.23
The Jackson Laboratory