About   Help   FAQ
Symbol
Name
ID
Nsdhl
NAD(P) dependent steroid dehydrogenase-like
MGI:1099438
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Umbilical hernia
Short stature
Slender build
Mild intrauterine growth retardation
Disease(s) Associated with NSDHL
CHILD syndrome
CK syndrome

Mouse Phenotypes
embryonic growth retardation
decreased embryo size
decreased body weight
decreased body size
postnatal growth retardation
Availability Mouse Genotype
NsdhlBpa-1H/Nsdhl+
NsdhlBpa-5H/Nsdhl+
NsdhlBpa-8H/Nsdhl+
NsdhlBpa-1H/Y
NsdhlBpa-8H/Y
NsdhlStr-1H/Y
Nsdhltm1.1Hrm/Nsdhl+
Edil3Tg(Sox2-cre)1Amc/Edil3+  (conditional)
Nsdhltm1.1Hrm/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+  (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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory