SHFM1
Template:PBB 26S proteasome complex subunit DSS1 is a protein that in humans is encoded by the SHFM1 gene.[1][2][3]
Interactions
SHFM1 has been shown to interact with BRCA2.[4][5]
References
- ^ Roberts SH, Hughes HE, Davies SJ, Meredith AL (October 1991). "Bilateral split hand and split foot malformation in a boy with a de novo interstitial deletion of 7q21.3". J Med Genet. 28 (7): 479–481. doi:10.1136/jmg.28.7.479. PMC 1016960. PMID 1895319.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, Soder S, Cobben JM, Hudgins L, Evans JP, Tsui LC (June 1997). "Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development". Hum Mol Genet. 5 (5): 571–579. doi:10.1093/hmg/5.5.571. PMID 8733122.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: SHFM1 split hand/foot malformation (ectrodactyly) type 1".
- ^ Marston, N J; Richards W J; Hughes D; Bertwistle D; Marshall C J; Ashworth A (July 1999). "Interaction between the product of the breast cancer susceptibility gene BRCA2 and DSS1, a protein functionally conserved from yeast to mammals". Mol. Cell. Biol. 19 (7). UNITED STATES: 4633–42. ISSN 0270-7306. PMC 84261. PMID 10373512.
- ^ Yang, Haijuan; Jeffrey Philip D; Miller Julie; Kinnucan Elspeth; Sun Yutong; Thoma Nicolas H; Zheng Ning; Chen Phang-Lang; Lee Wen-Hwa; Pavletich Nikola P (September 2002). "BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure". Science. 297 (5588). United States: 1837–1848. doi:10.1126/science.297.5588.1837. PMID 12228710.
Further reading
PDB gallery | |
|---|---|
|
 | This article on a gene on human chromosome 7 is a stub. You can help Wikipedia by expanding it. |