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Ccdc136Gt(373F8)Cmhd
Gene trapped Allele Detail
Summary
Symbol: Ccdc136Gt(373F8)Cmhd
Name: coiled-coil domain containing 136; gene trap 373F8, Centre for Modeling Human Disease
MGI ID: MGI:4965479
Synonyms: Ccdc136GFP
Gene: Ccdc136  Location: Chr6:29396296-29426954 bp, + strand  Genetic Position: Chr6, 12.36 cM
Alliance: Ccdc136Gt(373F8)Cmhd page
Mutation
origin
Mutant Cell Line:  373F8
Germline Transmission:  Earliest citation of germline transmission: J:249375
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Gene trapped
Mutation:    Insertion of gene trap vector     Vector: UPA
 
Mutation detailsThe gene was disrupted by the insertion of a pUPA GFP reporter vector 3' to exon 2 in the gene. The detection of low levels of potentially functional transcripts in homozygous mice raised the possibility that this mutation is not a null allele. (J:249375)
Sequence Tags: 
Sequence tag details (1 tag)
Genome Context: 
Genome Browser view of this mutation
Expression
In Mice Carrying this Mutation: 81 assay results
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 Ccdc136 Mutation:  33 strains or lines available
References
Original:  J:141210 Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI), Mouse Gene Trap Data Load from dbGSS. Database Download. 2008;
All:  4 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
05/14/2024
MGI 6.23
The Jackson Laboratory