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conls
Spontaneous Allele Detail
Summary
Symbol: conls
Name: coneless
MGI ID: MGI:6198566
Synonyms: conelessmut
Gene: conls  Location: unknown  
Alliance: conls page
Mutation
origin
Strain of Origin:  HsdWin:NMRI
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
 
Mutation detailsScreening of mice of the HsdWin:NMRI stock for ocular phenotypes identified some animals with little or no photoreceptor cone-derived electroretinograhy (ERG) signal. Analysis of several pedigrees showed this phenotype to be inherited in a monogenic, autosomal recessive manner. (J:82809)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any conls Mutation:  2 strains or lines available
References
Original:  J:82809 European Mouse Mutant Archive, Information obtained from the European Mouse Mutant Archive (EMMA). Unpublished. 2003-2013;
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