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Symbol
Name
ID
Spint2
serine protease inhibitor, Kunitz type 2
MGI:1338031
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Polyhydramnios
Disease(s) Associated with SPINT2
congenital secretory sodium diarrhea 3

Mouse Phenotypes
abnormal gastrulation
abnormal ectoderm development
abnormal neural tube morphology
abnormal neural tube closure
Availability Mouse Genotype
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg

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
04/30/2024
MGI 6.23
The Jackson Laboratory