Split Hand/foot Malformation (Ectrodactyly) Type 1 蛋白
(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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4 results :
SHFM1
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
> 85% by SDS-PAGE
SDS
1 image
Aliases for Split Hand/foot Malformation (Ectrodactyly) Type 1 蛋白
SEM1, 26S proteasome complex subunit (SEM1) 蛋白SEM1, 26S proteasome complex subunit (Sem1) 蛋白
SEM1, 26S proteasome complex subunit S homeolog (sem1.S) 蛋白
SEM1, 26S proteasome complex subunit (sem1) 蛋白
DSS1 蛋白
Dss1 蛋白
dss1 蛋白
ECD 蛋白
ecd 蛋白
SEM1 蛋白
sem1 蛋白
SHFD1 蛋白
shfd1 蛋白
Shfdg1 蛋白
shfdg1 蛋白
Shfg 蛋白
SHFM1 蛋白
shfm1 蛋白
shfm1.S 蛋白
SHSF1 蛋白
shsf1 蛋白
wu:fb55c02 蛋白
zgc:56203 蛋白
zgc:85901 蛋白
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