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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pou4f2tm4(DTA)Whk
targeted mutation 4, William H Klein
MGI:3838536
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Opn4tm1.1(cre)Saha/Opn4+
Pou4f2tm4(DTA)Whk/Pou4f2+
Tg(CAG-Bgeo/ALPP)1Lbe/0
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5285913
cn2
Opn4tm1.1(cre)Saha/Opn4+
Pou4f2tm4(DTA)Whk/Pou4f2+
involves: 129S/SvEv * C57BL/6 MGI:5285914
cn3
Opn4tm1.1(cre)Saha/Opn4tm1Yau
Pou4f2tm4(DTA)Whk/Pou4f2+
involves: 129S/SvEv * C57BL/6 MGI:5285915
cn4
Pou4f2tm4(DTA)Whk/Pou4f2+
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129S/SvEv * C57BL/6 * CBA MGI:3838797
cn5
Pou4f2tm4(DTA)Whk/Pou4f2tm4(DTA)Whk
Tg(Six3-cre)69Frty/?
involves: 129S/SvEv * C57BL/6 * DBA/2 MGI:3838794


Genotype
MGI:5285913
cn1
Allelic
Composition
Opn4tm1.1(cre)Saha/Opn4+
Pou4f2tm4(DTA)Whk/Pou4f2+
Tg(CAG-Bgeo/ALPP)1Lbe/0
Genetic
Background
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Opn4tm1.1(cre)Saha mutation (0 available); any Opn4 mutation (33 available)
Pou4f2tm4(DTA)Whk mutation (1 available); any Pou4f2 mutation (7 available)
Tg(CAG-Bgeo/ALPP)1Lbe mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• and olivary pretectal nucleus (OPN) projections are eliminated, compared to controls
• innervation of the intergeniculate leaflet (IGL) is markedly reduced
• all non-M1 retinal ganglion cells are ablated in the retinas, with only about 200 Pou4f2-negative cells detected (200/2000); these remaining fibers innervated the SCN to the same extent as control Pou4f2tm2.1Nat/+ Opn4tm1.1(cre)Saha/+ animals

vision/eye
• all non-M1 retinal ganglion cells are ablated in the retinas, with only about 200 Pou4f2-negative cells detected (200/2000); these remaining fibers innervated the SCN to the same extent as control Pou4f2tm2.1Nat/+ Opn4tm1.1(cre)Saha/+ animals




Genotype
MGI:5285914
cn2
Allelic
Composition
Opn4tm1.1(cre)Saha/Opn4+
Pou4f2tm4(DTA)Whk/Pou4f2+
Genetic
Background
involves: 129S/SvEv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Opn4tm1.1(cre)Saha mutation (0 available); any Opn4 mutation (33 available)
Pou4f2tm4(DTA)Whk mutation (1 available); any Pou4f2 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mutants are able to photoentrain (their circadian phase) like controls; also, activity
• the papillary light reflex (PLR) is significantly attenuated at high and low light intensities in the middle of the day (zeitgerber time 8, ZT8); in the middle of the night (ZT20), mice show no PLR
• animals show a minor deficit in period lengthening under constant light conditions

nervous system
• only 200 M1 (Pou4f2-negative) ipRGCs (intrinsically photosensitive retinal ganglion cells) are detected in the retinas

vision/eye
N
• visual acuity is comparable to wild-type animals
• the papillary light reflex (PLR) is significantly attenuated at high and low light intensities in the middle of the day (zeitgerber time 8, ZT8); in the middle of the night (ZT20), mice show no PLR
• only 200 M1 (Pou4f2-negative) ipRGCs (intrinsically photosensitive retinal ganglion cells) are detected in the retinas




Genotype
MGI:5285915
cn3
Allelic
Composition
Opn4tm1.1(cre)Saha/Opn4tm1Yau
Pou4f2tm4(DTA)Whk/Pou4f2+
Genetic
Background
involves: 129S/SvEv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Opn4tm1.1(cre)Saha mutation (0 available); any Opn4 mutation (33 available)
Opn4tm1Yau mutation (0 available); any Opn4 mutation (33 available)
Pou4f2tm4(DTA)Whk mutation (1 available); any Pou4f2 mutation (7 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• and olivary pretectal nucleus (OPN) projections are eliminated, compared to controls
• no fibres are observed in the shell of the OPN
• innervation of the intergeniculate nucleus (IGL) is markedly reduced
• only 200 M1 (Pou4f2-negative) ipRGCs (intrinsically photosensitive retinal ganglion cells) are detected in the retinas; these remaining fibers innervated the SCN to the same extent as control Pou4f2tm2.1Nat/+ ;Opn4tm1.1(cre)Saha/+ animals

vision/eye
• only 200 M1 (Pou4f2-negative) ipRGCs (intrinsically photosensitive retinal ganglion cells) are detected in the retinas; these remaining fibers innervated the SCN to the same extent as control Pou4f2tm2.1Nat/+ ;Opn4tm1.1(cre)Saha/+ animals




Genotype
MGI:3838797
cn4
Allelic
Composition
Pou4f2tm4(DTA)Whk/Pou4f2+
Tg(CAG-cre/Esr1*)5Amc/0
Genetic
Background
involves: 129S/SvEv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou4f2tm4(DTA)Whk mutation (1 available); any Pou4f2 mutation (7 available)
Tg(CAG-cre/Esr1*)5Amc mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• reduced cross-sectional area by 48.8% in 3 months after a 5 day course of tamoxifen treatment
• cross-sectional area reduced to 19.7% of controls at ten months after a 5 day course of tamoxifen treatment
• axons disorganized
• progressive degeneration over the course of ten months after a 5 day course of tamoxifen treatment
• severe axon degeneration and vacuolation
• empty or abnormal myelin sheaths
• 60% reduction in the number of cells of the ganglion layer one month after a 5 day course of tamoxifen treatment
• 33% of time spent in the light as opposed to 6% for controls after 1-2 hours of dark adaptation

nervous system
• reactive gliosis triggered one month after a 5 day course of tamoxifen treatment
• reduced cross-sectional area by 48.8% in 3 months after a 5 day course of tamoxifen treatment
• cross-sectional area reduced to 19.7% of controls at ten months after a 5 day course of tamoxifen treatment
• axons disorganized
• progressive degeneration over the course of ten months after a 5 day course of tamoxifen treatment
• severe axon degeneration and vacuolation
• empty or abnormal myelin sheaths




Genotype
MGI:3838794
cn5
Allelic
Composition
Pou4f2tm4(DTA)Whk/Pou4f2tm4(DTA)Whk
Tg(Six3-cre)69Frty/?
Genetic
Background
involves: 129S/SvEv * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou4f2tm4(DTA)Whk mutation (1 available); any Pou4f2 mutation (7 available)
Tg(Six3-cre)69Frty mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• clearly abnormal in 16 day old mice
• thinner with smaller diameter fibers
• unmyelinated fibers
• deformed at E14.5
• overall structure remains normal through 5 months of age
• reduced cell proliferation and increased apoptosis
• more than 98% of retinal ganglion cells ablated at E14.5
• only displaced amacrine cells present at 16 days of age
• noticeably thinner at E14.5
• 30-50% thinner than controls at 16 days of age
• saturated amplitudes of both light and dark adapted b-waves 25% of normal
• dark adapted a-wave amplitude 42% of normal
• negative scotopic threshold response is very small
• positive scotopic threshold response is absent

nervous system
• clearly abnormal in 16 day old mice
• thinner with smaller diameter fibers
• unmyelinated fibers
• deformed at E14.5





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory