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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Elp1tm1c(KOMP)Wtsi
targeted mutation 1c, Wellcome Trust Sanger Institute
MGI:5558022
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi
Tg(Ddx4-cre)1Dcas/0
involves: 129 * C57BL/6N * FVB MGI:7509348
cn2
Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: C57BL/6J * C57BL/6N * CBA/J MGI:5558037


Genotype
MGI:7509348
cn1
Allelic
Composition
Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi
Tg(Ddx4-cre)1Dcas/0
Genetic
Background
involves: 129 * C57BL/6N * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Elp1tm1c(KOMP)Wtsi mutation (0 available); any Elp1 mutation (69 available)
Tg(Ddx4-cre)1Dcas mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• impairment of meiotic progression in male germ cells takes place between zygotene to pachytene stage

homeostasis/metabolism

endocrine/exocrine glands
• testicular weight to body weight ratio was reduced by 25% at the age of 14 month

reproductive system
• impairment of meiotic progression in male germ cells takes place between zygotene to pachytene stage
• testicular weight to body weight ratio was reduced by 25% at the age of 14 month




Genotype
MGI:5558037
cn2
Allelic
Composition
Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: C57BL/6J * C57BL/6N * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Elp1tm1c(KOMP)Wtsi mutation (0 available); any Elp1 mutation (69 available)
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Reduced numbers of sympathetic and dorsal root ganglia neurons in Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi H2az2Tg(Wnt1-cre)11Rth/0 fetuses

mortality/aging
• die within 24 h of birth

nervous system
• premature differentiation of TrkA progenitors during the second wave of neurogenesis
• nearly a 70% decrease in the number of TH+ neurons in the superior cervical ganglion at E17.5
• central projections of TrkA+ dorsal root ganglia neurons are considerably reduced in the dorsal horn of the spinal cord
• decrease in the prevalence of TrkA+ fibers in the skin at E17.5
• TH+ sympathetic terminals rarely innervate the parasympathetic cell bodies in the submandibular gland
• decrease in the total number and number of TrkA+ dorsal root ganglia neurons at E10.5 and E12.5 but not at E11.5
• nearly a 70% decrease in the number of TH+ neurons in the superior cervical ganglion at E17.5
• the total number of dorsal root ganglia neurons are reduced by 1/3 at E17.5
• a 50% decrease in the number of pain- and temperature-receptive neurons at E17.5
• slight but significant increase in the number of TrkC expressing neurons (mechanoreceptors) in the dorsal root ganglia
• decrease in the total number of dorsal root ganglia neurons at E10.5
• the total number of dorsal root ganglia neurons are reduced by 1/3 at E17.5
• neurons transiently expressing TH (possible future thermal pain receptors) are virtually absent
• slight but significant increase in the number of TrkC expressing neurons (mechanoreceptors)
• substance P is virtually absent in the dorsal root ganglia
• in the superior cervical ganglion and dorsal root ganglia at E17.5
• in the dorsal root ganglia at E12.5 and E17.5

craniofacial
• increased mandibular retroposition
• decreased inferior facial angle

growth/size/body
• decreased inferior facial angle

digestive/alimentary system
• parasympathetic cell bodies are reduced by 31%

skeleton
• increased mandibular retroposition

cellular
• in the superior cervical ganglion and dorsal root ganglia at E17.5
• in the dorsal root ganglia at E12.5 and E17.5
• premature differentiation of TrkA progenitors during the second wave of neurogenesis

endocrine/exocrine glands
• parasympathetic cell bodies are reduced by 31%

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Riley-Day syndrome DOID:11589 OMIM:223900
J:202989





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory