Symbol Name ID Chromosome |
Scd1
stearoyl-Coenzyme A desaturase 1 MGI:98239 19 |
Experiment Type | Details | Chromosome | Reference |
---|---|---|---|
CROSS |
Cross Type: Intercross |
19 | J:7870 Marks SC Jr, et al., Osteosclerosis, a recessive skeletal mutation on chromosome 19 in the mouse. J Hered. 1985 May-Jun;76(3):171-6 |
CROSS |
Cross Type: Intercross |
19 | J:23682 Sweet HO, Osteochondrodystrophy (ocd) (Correction: Mouse News Lett 1989; 83:168). Mouse News Lett. 1988;81:70 |
CROSS |
Cross Type: Intercross |
19 | J:23682 Sweet HO, Osteochondrodystrophy (ocd) (Correction: Mouse News Lett 1989; 83:168). Mouse News Lett. 1988;81:70 |
CROSS |
Cross Type: Backcross |
19 | J:23682 Sweet HO, Osteochondrodystrophy (ocd) (Correction: Mouse News Lett 1989; 83:168). Mouse News Lett. 1988;81:70 |
CROSS |
Cross Type: Backcross |
19 | J:23682 Sweet HO, Osteochondrodystrophy (ocd) (Correction: Mouse News Lett 1989; 83:168). Mouse News Lett. 1988;81:70 |
CROSS |
Cross Type: Intercross |
19 | J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4 |
CROSS |
Cross Type: Intercross |
19 | J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4 |
CROSS |
Cross Type: Backcross |
19 | J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4 |
CROSS |
Cross Type: Backcross |
19 | J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4 |
CROSS |
Cross Type: Backcross |
19 | J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4 |
CROSS |
Cross Type: Single backcross |
19 | J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4 |
CROSS |
Cross Type: Backcross |
19 | J:41734 Tabor DE, et al., A cluster of stearoyl CoA desaturase genes, Scd1 and Scd2, on mouse chromosome 19. Mamm Genome. 1997;9:341-342 |
TEXT | 19 | J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20 | |
TEXT | 19 | J:93033 Lu Y, et al., Scd1( ab-Xyk): a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse. Mol Genet Genomics. 2004 Sep;272(2):129-37 | |
TEXT-Genetic Cross | 19 | J:42484 Gardner JM, et al., The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9238-43 | |
TEXT-Genetic Cross | 19 | J:54055 Ji W, et al., Identification of genes within the Krd deletion on mouse chromosome 19. Mamm Genome. 1999 Apr;10(4):399-401 | |
TEXT-Genetic Cross | 19 | J:56862 Richardson M, et al., Mouse Wnt8B is expressed in the developing forebrain and maps to chromosome 19. Mamm Genome. 1999 Sep;10(9):923-5 | |
TEXT-Genetic Cross | 19 | J:13725 Sweet HO, et al., [Asebia-J on Chromosome 19.]. Mouse News Lett. 1977;57:20 | |
TEXT-Genetic Cross | 19 | J:20207 Sweet HO, et al., Linkage data: Tail short (Ts) is linked to Rex (Re). Mouse News Lett. 1978;59:27 | |
TEXT-Physical Mapping | 19 | J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573 | |
TEXT-Physical Mapping | 19 | J:67579 Zheng Y, et al., Scd3-a novel gene of the stearoyl-coa desaturase family with restricted expression in skin. Genomics. 2001 Jan 15;71(2):182-91 | |
TEXT-QTL | 19 | J:123776 Wergedal JE, et al., Mapping genetic loci that regulate lipid levels in a NZB/B1NJxRF/J intercross and a combined intercross involving NZB/B1NJ, RF/J, MRL/MpJ, and SJL/J mouse strains. J Lipid Res. 2007 Aug;48(8):1724-34 | |
TEXT-QTL-Candidate Genes | 19 | J:80006 Falvella FS, et al., Stearoyl-CoA desaturase 1 (Scd1) gene overexpression is associated with genetic predisposition to hepatocarcinogenesis in mice and rats. Carcinogenesis. 2002 Nov;23(11):1933-6 | |
TEXT-QTL-Candidate Genes | 19 | J:98587 Hitzemann R, et al., On the integration of alcohol-related quantitative trait loci and gene expression analyses. Alcohol Clin Exp Res. 2004 Oct;28(10):1437-48 | |
TEXT-Radiation Hybrid | 19 | J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004; |
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 11/12/2024 MGI 6.24 |
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