Symbol Name ID |
Nsdhl
NAD(P) dependent steroid dehydrogenase-like MGI:1099438 |
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 |
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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) |
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Nsdhltm1.1Hrm/Y Edil3Tg(Sox2-cre)1Amc/Edil3+ (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 09/03/2024 MGI 6.24 |
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