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Shfm1split hand/foot malformation (ectrodactyly) type 1 |
Known also as: DSS1; Shfg; Shfdg1;
| NCBI Gene ID: | 20422 |
| NCBI Ensembl Id: | ENSMUSG00000042541 |
| Species: | Mus musculus |
| Mus musculus split hand/foot malformation (ectrodactyly) type 1 (Shfm1). |
Gene sequence:
| [Download sequence] |
Proteins coded by this gene:
References:
| Authors | Title | Journal |
| Yang H, Jeffrey PD, Miller J, Kinnucan E, Sun Y, Thoma NH, Zheng N, Chen PL, Lee WH, Pavletich NP | BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure. | Science Sept. 13, 2002 |
| Gudmundsdottir K, Lord CJ, Witt E, Tutt AN, Ashworth A | DSS1 is required for RAD51 focus formation and genomic stability in mammalian cells. | EMBO Rep Oct. 1, 2004 |
| Katayama S, Tomaru Y, Kasukawa T, Waki K, Nakanishi M, Nakamura M, Nishida H, Yap CC, Suzuki M, Kawai J, Suzuki H, Carninci P, Hayashizaki Y, Wells C, Frith M, Ravasi T, Pang KC, Hallinan J, Mattick J, Hume DA, Lipovich L, Batalov S, Engstrom PG, Mizuno Y, Faghihi MA, Sandelin A, Chalk AM, Mottagui-Tabar S, Liang Z, Lenhard B, Wahlestedt C | Antisense transcription in the mammalian transcriptome. | Science Sept. 2, 2005 |
| Krizhanovsky V, Soreq L, Kliminski V, Ben-Arie N | Math1 target genes are enriched with evolutionarily conserved clustered E-box binding sites. | J Mol Neurosci Jan. 1, 2006 |
| Ono R, Nakamura K, Inoue K, Naruse M, Usami T, Wakisaka-Saito N, Hino T, Suzuki-Migishima R, Ogonuki N, Miki H, Kohda T, Ogura A, Yokoyama M, Kaneko-Ishino T, Ishino F | Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality. | Nat Genet Feb. 1, 2006 |
Last modification of this entry: Oct. 6, 2010.
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