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See other SHFM1 GE Assays ›
Gene Symbol:
SHFM1
Gene Name:
split hand/foot malformation (ectrodactyly) type 1
Gene Aliases:
DSS1, ECD, SEM1, SHFD1, SHSF1, Shfdg1
Chromosome Location:
Chr.7: 96688767 - 96709891 on Build GRCh38
Species:
Human
Species Specific ID (Flybase ID):
-
Assay ID Hs02793401_g1
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Catalog # 4351372
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  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

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Assay Details

Gene Symbol: SHFM1
Interrogated Sequence Translated Protein Exon Boundary Assay Location IMAGE Clone ID Amplicon Length
RefSeq NM_006304.1 NP_006295.1 1 - 2 205 77
GenBank mRNA AK291070.1 - 1 - 2 185 77
AK309241.1 - 1 - 2 163 77
BC032782.1 - 1 - 2 165 5166837 77
CR456887.1 - 1 - 2 77 77
U41515.1 - 1 - 2 205 77

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More Information


Set Membership:

Ambion siRNA available Amplicon length between 71 and 85 Mammalian Gene Collection Detect Genomic DNA Recommended Assay Homo sapiens Probe spans exons

Matching Ambion siRNAs:

Click here to find siRNAs for Gene SHFM1

Panther Classification:

Molecular Function -

protease protein modifying enzyme

Gene Ontology Categories:

Function(s) Process(es)

double-strand break repair via homologous recombination
mRNA export from nucleus
proteolysis
proteasome assembly
protein binding

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