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Symbol
Name
ID
Gja1
gap junction protein, alpha 1
MGI:95713
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Maternal diabetes
Abnormality of chromosome segregation
Hypoglycemia
Diabetes mellitus
Cerebral calcification
Basal ganglia calcification
Disease(s) Associated with GJA1
erythrokeratodermia variabilis
hypoplastic left heart syndrome
oculodentodigital dysplasia

Mouse Phenotypes
abnormal vascular wound healing
abnormal blood homeostasis
abnormal circulating hormone level
cyanosis
edema
lymphedema
impaired skin barrier function
Availability Mouse Genotype
Gja1tm1Kdr/Gja1tm1Kdr
Gja1tm3.1Clo/Gja1tm3.1Clo
Gja1tm4Kwi/Gja1tm4Kwi
Gja1tm1Dlg/Gja1tm1Dlg
Tg(Tek-cre)1Ywa/0  (conditional)
Gja1tm1Kwi/Gja1+
Tg(KRT5-cre)5132Jlj/0  (conditional)
Gja1tm1Kwi/Gja1tm5(cre/ERT)Kwi  (conditional)

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