Symbol Name ID |
Atrx
ATRX, chromatin remodeler MGI:103067 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Feeding difficulties in infancy |
Poor suck |
Depression |
Atypical behavior |
Autism |
Motor stereotypy |
Self-injurious behavior |
Weak cry |
Fatigue |
Disease(s) Associated with ATRX | |||||||||
alpha thalassemia-X-linked intellectual disability syndrome | |||||||||
alpha-thalassemia myelodysplasia syndrome |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal behavior |
impaired contextual conditioning behavior |
absent gastric milk in neonates |
abnormal suckling behavior |
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Availability | Mouse Genotype | |||||
Atrxtm1Enl/Atrxtm1Enl | * | |||||
Atrxtm1Rjg/Atrx+ Tg(Gata1-cre)1Sho/0 (conditional) |
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Atrxtm1Rjg/Y Foxg1tm1(cre)Skm/Foxg1+ (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 04/09/2024 MGI 6.23 |
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