Symbol Name ID |
Ercc5
excision repair cross-complementing rodent repair deficiency, complementation group 5 MGI:103582 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Small for gestational age |
Growth delay |
Intrauterine growth retardation |
Disease(s) Associated with ERCC5 | |||
cerebrooculofacioskeletal syndrome 3 | |||
xeroderma pigmentosum group G |
Mouse Phenotypes | growth/size/body region phenotype |
postnatal growth retardation |
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Availability | Mouse Genotype | ||
Ercc5tm1Shm/Ercc5tm1Shm | |||
Ercc5tm2Shm/Ercc5tm2Shm | * | ||
Ercc5tm3Shm/Ercc5tm3Shm | |||
Ercc5tm4Shm/Ercc5tm4Shm | * |
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 |
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