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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Nsdhl
NAD(P) dependent steroid dehydrogenase-like
MGI:1099438
69 phenotypes from 11 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
NsdhlBpa-1H/Nsdhl+
involves: 101/H * C3H/HeH
abnormal coat/ hair morphology J:7012
abnormal digit morphology J:7012
abnormal hair shaft morphology J:7012
abnormal limb morphology J:7012
abnormal maternal nurturing J:5403
abnormal tail morphology J:7012
alopecia J:5403, J:7012
brachydactyly J:5403
brachypodia J:5403
cataract J:7012
clinodactyly J:5403
decreased body size J:5403
decreased body weight J:5403
disheveled coat J:5403, J:7012
hyperkeratosis J:7012
irregular coat pigmentation J:5403
kinked tail J:7012
perinatal lethality, incomplete penetrance J:95508
postnatal lethality, incomplete penetrance J:95508
premature endochondral bone ossification J:7012
short limbs J:7012
short tail J:7012
NsdhlBpa-1H/Y
involves: 101/H * C3H/HeH
abnormal vitelline vascular remodeling J:95508
decreased embryo size J:95508
disorganized placental labyrinth J:95508
embryonic growth retardation J:95508
pale yolk sac J:95508
pallor J:95508
prenatal lethality, complete penetrance J:5403, J:95508
small placenta J:95508
thin placenta labyrinth J:95508
NsdhlBpa-3H/Y
involves: 101/H * C3H/HeH
prenatal lethality, complete penetrance J:55488
NsdhlBpa-3H/Nsdhl+
involves: 101/H * C3H/HeH
abnormal skeleton morphology J:55488
abnormal skin condition J:90559
abnormal vertebral column morphology J:90559
focal hair loss J:90559
hyperkeratosis J:55488
irregular coat pigmentation J:55488
NsdhlBpa-4H/Nsdhl+
Not Specified
abnormal vertebral column morphology J:90559
alopecia J:90559
NsdhlBpa-4H/Y
Not Specified
prenatal lethality, complete penetrance J:90559
NsdhlBpa-5H/Nsdhl+
involves: 101/H * C3H/HeH
abnormal skeleton morphology J:55488
decreased body size J:90559
focal hair loss J:90559
hyperkeratosis J:55488
irregular coat pigmentation J:55488
short vertebral column J:90559
NsdhlBpa-5H/Y
involves: 101/H * C3H/HeH
prenatal lethality, complete penetrance J:55488
NsdhlBpa-6H/Y
involves: 101/H * C3H/HeH
prenatal lethality, complete penetrance J:55488
NsdhlBpa-6H/Nsdhl+
involves: 101/H * C3H/HeH
abnormal skeleton morphology J:55488
focal hair loss J:90559
hyperkeratosis J:55488
irregular coat pigmentation J:55488
NsdhlBpa-7H/Y
Not Specified
prenatal lethality J:100224
NsdhlBpa-7H/Nsdhl+
Not Specified
abnormal skin condition J:100224
alopecia J:100224
hyperkeratosis J:100224
NsdhlBpa-8H/Y
involves: BALB/c * C3H/HeN
abnormal forebrain morphology J:95508
abnormal placenta labyrinth morphology J:95508
abnormal vitelline vascular remodeling J:95508
decreased embryo size J:95508
disorganized placental labyrinth J:95508
embryonic growth retardation J:95508
embryonic lethality during organogenesis, complete penetrance J:95508
hemorrhage J:95508
pale yolk sac J:95508
pallor J:95508
pericardial effusion J:95508
prenatal lethality, complete penetrance J:90559, J:100224
small placenta J:95508
thin placenta labyrinth J:95508
NsdhlBpa-8H/Nsdhl+
involves: BALB/c * C3H/HeN
abnormal skin condition J:90559, J:100224
alopecia J:100224
decreased body size J:90559, J:95508
hyperkeratosis J:95508, J:100224
irregular coat pigmentation J:90559
NsdhlStr-1H/Y
involves: 101/H * C3H/HeH
abnormal placenta labyrinth morphology J:95508
abnormal vitelline vascular remodeling J:95508
decreased embryo size J:95508
disorganized placental labyrinth J:95508
embryonic growth retardation J:95508
embryonic lethality during organogenesis, complete penetrance J:290, J:55488, J:95508
hemorrhage J:95508
pale yolk sac J:95508
pallor J:95508
pericardial effusion J:95508
small placenta J:95508
thin placenta labyrinth J:95508
NsdhlStr-1H/Nsdhl+
involves: 101/H * C3H/HeH
abnormal auchene hair morphology J:55488
abnormal guard hair morphology J:55488
abnormal retina morphology J:106524
abnormal sweat gland morphology J:106524
irregular coat pigmentation J:290, J:55488
kyphosis J:106524
normal mortality/aging J:55488
retina degeneration J:106524
short hair J:55488
NsdhlStr-1Or/Nsdhl+
involves: 101/Rl * C3H/Rl
abnormal coat/ hair morphology J:100221
irregular coat pigmentation J:55488, J:100221
variable body spotting J:55488
NsdhlStr-1Or/Y
involves: 101/Rl * C3H/Rl
embryonic lethality during organogenesis, complete penetrance J:55488, J:95508
prenatal lethality, complete penetrance J:100221
small placenta J:95508
NsdhlStr-1Or/NsdhlStr-1Or
involves: 101/Rl * C3H/Rl
prenatal lethality, complete penetrance J:100221
NsdhlStr-2H/Y
involves: 101/H * C3H/HeH
embryonic lethality during organogenesis, complete penetrance J:55488, J:95508
NsdhlStr-2H/Nsdhl+
involves: 101/H * C3H/HeH
irregular coat pigmentation J:55488
variable body spotting J:55488
Nsdhltm1.1Hrm/Nsdhl+
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA
abnormal hair growth J:220990
abnormal skeleton morphology J:220990
decreased body size J:220990
hyperkeratosis J:220990
Nsdhltm1.1Hrm/Y
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA
postnatal growth retardation J:220990
Nsdhltm1.1Hrm/Y
Tg(GFAP-cre)25Mes/0
involves: 129S6/SvEvTac * C57BL/6J * FVB/N
abnormal Bergmann glial cell morphology J:220990
abnormal cerebellar granule cell morphology J:220990
abnormal cerebral cortex morphology J:220990
abnormal dentate gyrus morphology J:220990
abnormal hippocampus granule cell morphology J:220990
abnormal hippocampus morphology J:220990
abnormal hippocampus neuron morphology J:220990
abnormal neurite morphology J:220990
abnormal neuronal stem cell physiology J:220990
abnormal Purkinje cell dendrite morphology J:220990
ataxia J:220990
decreased cerebellar granule cell number J:220990
premature death J:220990
small cerebellum J:220990
small hippocampus J:220990
thin external granule cell layer J:220990

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
04/23/2024
MGI 6.23
The Jackson Laboratory