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Sema4aGt(OST393408)Lex
Gene trapped Allele Detail
Summary
Symbol: Sema4aGt(OST393408)Lex
Name: sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A; gene trap OST393408, Lexicon Genetics
MGI ID: MGI:3052925
Synonyms: Sema4aGt22Lex
Gene: Sema4a  Location: Chr3:88343266-88368489 bp, - strand  Genetic Position: Chr3, 38.83 cM
Alliance: Sema4aGt(OST393408)Lex page
Mutation
origin
Mutant Cell Line:  OST393408
Germline Transmission:  Earliest citation of germline transmission: J:92305
Parent Cell Line:  Lex-1 (ES Cell)
Strain of Origin:  129S5/SvEvBrd
Project Collection: Lexicon
Mutation
description
Allele Type:    Gene trapped (Null/knockout)
Mutation:    Insertion of gene trap vector
 
Mutation detailsA gene trap vector consisting of LTR sites and a Neo marker was inserted into intron 11 of the endogenous gene. RT-PCR analysis detected no endogenous transcript in the eyes of homozygous mice. (J:92305)
Sequence Tags: 
Sequence tag details (1 tag)
Genome Context: 
Genome Browser view of this mutation
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 7 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Sema4a Mutation:  39 strains or lines available
Notes
See also, data as provided by Lexicon Genetics, Inc.
References
Original:  J:92305 Rice DS, et al., Severe retinal degeneration associated with disruption of semaphorin 4A. Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2767-77
All:  3 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