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Symbol
Name
ID
Hsd17b4
hydroxysteroid (17-beta) dehydrogenase 4
MGI:105089
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties in infancy
Depression
Disease(s) Associated with HSD17B4
D-bifunctional protein deficiency
Stiff-Person syndrome

Mouse Phenotypes
behavior/neurological phenotype
lethargy
increased anxiety-related response
limb grasping
tremors
ataxia
impaired coordination
increased grip strength
abnormal gait
short stride length
Availability Mouse Genotype
Hsd17b4em1(IMPC)Tcp/Hsd17b4em1(IMPC)Tcp
Hsd17b4tm1Baes/Hsd17b4tm1Baes
Hsd17b4em1(IMPC)Tcp/Hsd17b4+
Hsd17b4tm2Baes/Hsd17b4tm2Baes
Cnptm1(cre)Kan/Cnp+  (conditional)
*
Hsd17b4tm2Baes/Hsd17b4tm2Baes
Tg(Nes-cre)1Kln/0  (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
04/16/2024
MGI 6.23
The Jackson Laboratory