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Symbol
Name
ID
Tctn2
tectonic family member 2
MGI:1915228
Phenotype annotations related to limbs/digits/tail
Darker colors indicate more annotations
Human Phenotypes
Postaxial hand polydactyly
Postaxial foot polydactyly
Polydactyly
Delayed proximal femoral epiphyseal ossification
Talipes equinovarus
Disease(s) Associated with TCTN2
Joubert syndrome 24
Meckel syndrome 8

Mouse Phenotypes
abnormal limb mesenchyme morphology
preaxial polydactyly
Availability Mouse Genotype
Tctn2tm1.1Reit/Tctn2tm1.1Reit

Contributing Projects:
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
The Jackson Laboratory