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| Nomenclature |
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Symbol:
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Htr2ctm1Jul
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Name:
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5-hydroxytryptamine (serotonin) receptor 2C;
targeted mutation 1, David Julius
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MGI ID: |
MGI:1857439 |
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Synonyms: |
5-HT2cR-deficient |
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Gene:
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Htr2c
Location:
ChrX:146962513-147197277 bp, + strand
Genetic Position: ChrX,
68.46 cM, cytoband D-F4
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:24339
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Parent Cell Line:
| Other (see notes) (ES Cell) |
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Strain of Origin:
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129S/Sv
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Nucleotide substitutions |
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Mutation details: Insertion of a nonsense mutation into exon 5 of the gene resulted in the introduction of a stop codon within the fifth putative transmembrane segment of the receptor and in the elimination of the carboxy-terminal half of the protein. (J:24339)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Notes |
ES cell line = D3 (129S2/SvPas) or J1 (129S4/SvJae).
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| References |
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Original: |
J:24339
Tecott LH et al.,
"Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors [see comments]"
Nature 1995 Apr 6;374(6522):542-6
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All: |
31 reference(s)
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