Human Gene SNX11 (ENST00000359238.7) from GENCODE V44
Description: Homo sapiens sorting nexin 11 (SNX11), transcript variant 2, mRNA. (from RefSeq NM_013323) RefSeq Summary (NM_013323): This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. This gene encodes a protein of unknown function. This gene results in two transcript variants differing in the 5' UTR, but encoding the same protein. [provided by RefSeq, Jul 2008]. Gencode Transcript: ENST00000359238.7 Gencode Gene: ENSG00000002919.15 Transcript (Including UTRs) Position: hg38 chr17:48,107,766-48,123,601 Size: 15,836 Total Exon Count: 7 Strand: + Coding Region Position: hg38 chr17:48,112,044-48,121,508 Size: 9,465 Coding Exon Count: 6
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 Q9Y5W9
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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
