Human Gene SLC47A1 (ENST00000436810.6) from GENCODE V44
Description: The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data. (from UniProt E7EX57) RefSeq Summary (NM_018242): This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]. Gencode Transcript: ENST00000436810.6 Gencode Gene: ENSG00000142494.13 Transcript (Including UTRs) Position: hg38 chr17:19,533,828-19,577,611 Size: 43,784 Total Exon Count: 15 Strand: + Coding Region Position: hg38 chr17:19,533,940-19,577,336 Size: 43,397 Coding Exon Count: 15
ID:E7EX57_HUMAN DESCRIPTION: SubName: Full=Multidrug and toxin extrusion protein 1; CAUTION: The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
ModBase Predicted Comparative 3D Structure on E7EX57
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Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
US Server
