Symbol Name ID |
Gja1
gap junction protein, alpha 1 MGI:95713 |
* | Aspects of the system are reported to show a normal phenotype. |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Photophobia |
Disease(s) Associated with GJA1 | |
palmoplantar keratoderma and congenital alopecia 1 |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal behavior |
abnormal suckling behavior |
poor grooming |
abnormal motor capabilities/coordination/movement |
ataxia |
abnormal gait |
|
Availability | Mouse Genotype | |||||||
Gja1tm1Kdr/Gja1tm1Kdr | ||||||||
Gja1M1Jrt/Gja1+ | * | |||||||
Gja1tm1Dlg/Gja1tm1Dlg Tg(GFAP-cre)1Kdmc/0 (conditional) |
! | |||||||
Gja1tm1Kwi/Gja1tm1Kwi Tg(S100b-cre)20Ito/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 04/16/2024 MGI 6.23 |
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