Split Hand/foot Malformation (Ectrodactyly) Type 1 抗体
(Split Hand/foot Malformation (Ectrodactyly) Type 1 (SHFM1))
The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008].
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Latest Publications for our Split Hand/foot Malformation (Ectrodactyly) Type 1 抗体
: "Identification of Dss1 as a 12-O-tetradecanoylphorbol-13-acetate-responsive gene expressed in keratinocyte progenitor cells, with possible involvement in early skin tumorigenesis." in: The Journal of biological chemistry, Vol. 278, Issue 3, pp. 1758-68, (2003) (PubMed).: "BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure." in: Science (New York, N.Y.), Vol. 297, Issue 5588, pp. 1837-48, (2002) (PubMed).
Aliases for Split Hand/foot Malformation (Ectrodactyly) Type 1 抗体
SEM1, 26S proteasome complex subunit (SEM1) 抗体SEM1, 26S proteasome complex subunit (Sem1) 抗体
SEM1, 26S proteasome complex subunit S homeolog (sem1.S) 抗体
SEM1, 26S proteasome complex subunit (sem1) 抗体
DSS1 抗体
Dss1 抗体
dss1 抗体
ECD 抗体
ecd 抗体
SEM1 抗体
sem1 抗体
SHFD1 抗体
shfd1 抗体
Shfdg1 抗体
shfdg1 抗体
Shfg 抗体
SHFM1 抗体
shfm1 抗体
shfm1.S 抗体
SHSF1 抗体
shsf1 抗体
wu:fb55c02 抗体
zgc:56203 抗体
zgc:85901 抗体
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