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Nme7Gt(OST31116)Lex
Gene trapped Allele Detail
Nomenclature
Symbol: Nme7Gt(OST31116)Lex
Name: NME/NM23 family member 7; gene trap OST31116, Lexicon Genetics
MGI ID: MGI:4151115
Gene: Nme7  Location: Chr1:164312879-164348181 bp, + strand  Genetic Position: Chr1, 71.63 cM
Mutation
origin
Mutant Cell Line:  OST31116 (Lexicon Genetics)
Germline Transmission:  Earliest citation of germline transmission: J:171184
Parent Cell Line:  Lex-1 (ES Cell)
Strain of Origin:  129S5/SvEvBrd
Project Collection: Lexicon
Mutation
description
Allele Type:    Gene trapped
Mutation:    Insertion of gene trap vector
    Gene trap insertion was in intron 1. (J:171184)
Sequence Tags: 
Sequence tag details (1 tag)
Genome Context: 
Genome Browser view of this mutation
Phenotypes
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View phenotypes 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 Nme7 Mutation:  25 strains or lines available
Notes
Phenotypic Similarity to Human Syndrome: Hydrocephalus in homozygous mice (J:185566)

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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/09/2014
MGI 5.20
The Jackson Laboratory