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Ecsitmpc178H
Chemically induced Allele Detail
Summary
Symbol: Ecsitmpc178H
Name: ECSIT signalling integrator; muta-ped-c3pde 178, Harwell
MGI ID: MGI:5503987
Gene: Ecsit  Location: Chr9:21983542-21996734 bp, - strand  Genetic Position: Chr9, 8.23 cM, cytoband A4
Alliance: Ecsitmpc178H page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Harwell ENU Mutagenesis
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced an A to T point mutation that results in the amino acid substitution of isoleucine for asparagine at position 209 (N209I). (J:234901)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Ecsit Mutation:  13 strains or lines available
References
Original:  J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
All:  1 reference(s)

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