Symbol Name ID |
Atrx
ATRX, chromatin remodeler MGI:103067 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Umbilical hernia |
Short stature |
Growth delay |
Postnatal growth retardation |
Disease(s) Associated with ATRX | |||||
alpha thalassemia-X-linked intellectual disability syndrome | |||||
alpha-thalassemia myelodysplasia syndrome |
Mouse Phenotypes | embryonic growth retardation |
decreased embryo size |
decreased birth body size |
decreased body weight |
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Availability | Mouse Genotype | ||||
Atrxtm1Enl/Atrxtm1Enl | |||||
Atrxtm1Rjg/Y Foxg1tm1(cre)Skm/Foxg1+ (conditional) |
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Atrxtm1Rjg/Y Tg(Nes-cre)2472Pick/0 (conditional) |
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Atrxtm1Rjg/Y Tg(Gata1-cre)1Sho/0 (conditional) |
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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