Symbol Name ID |
Atrx
ATRX, chromatin remodeler MGI:103067 |
Darker colors indicate more annotations |
Human Phenotypes | Death in infancy |
Disease(s) Associated with ATRX | |
alpha thalassemia-X-linked intellectual disability syndrome |
Mouse Phenotypes | postnatal lethality, complete penetrance |
postnatal lethality, incomplete penetrance |
embryonic lethality during organogenesis, complete penetrance |
embryonic lethality during organogenesis, incomplete penetrance |
prenatal lethality, incomplete penetrance |
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Availability | Mouse Genotype | |||||
Atrxtm1Enl/Atrxtm1Enl | ||||||
AtrxGt(E085A04)Wrst/Y | ||||||
Atrxtm1Rjg/Atrx+ Tg(Gata1-cre)1Sho/0 (conditional) |
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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 07/05/2024 MGI 6.24 |
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