Symbol Name ID |
Ptpn11
protein tyrosine phosphatase, non-receptor type 11 MGI:99511 |
Darker colors indicate more annotations |
Human Phenotypes | Bruising susceptibility |
Low posterior hairline |
Preauricular pit |
Wide intermamillary distance |
Abnormal hair quantity |
Coarse hair |
Woolly hair |
Cafe-au-lait spot |
Multiple lentigines |
Melanocytic nevus |
Dry skin |
Abnormal dermatoglyphics |
Disease(s) Associated with PTPN11 | ||||||||||||
Noonan syndrome | ||||||||||||
Noonan syndrome 1 | ||||||||||||
Noonan syndrome with multiple lentigines 1 | ||||||||||||
tetralogy of Fallot |
Mouse Phenotypes | decreased subcutaneous adipose tissue amount |
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Availability | Mouse Genotype | |
Ptpn11tm1.1Ics/Ptpn11+ |
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 04/16/2024 MGI 6.23 |
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