About   Help   FAQ
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 (68 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 (68 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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory