Human Gene ANXA11 (ENST00000438331.5) from GENCODE V44
Description: Homo sapiens annexin A11 (ANXA11), transcript variant c, mRNA. (from RefSeq NM_145869) RefSeq Summary (NM_145869): This gene encodes a member of the annexin family, a group of calcium-dependent phospholipid-binding proteins. Annexins have unique N-terminal domains and conserved C-terminal domains, which contain calcium-dependent phospholipid-binding sites. The encoded protein is a 56-kD antigen recognized by sera from patients with various autoimmune diseases. Several transcript variants encoding two different isoforms have been identified. [provided by RefSeq, Dec 2015]. Gencode Transcript: ENST00000438331.5 Gencode Gene: ENSG00000122359.18 Transcript (Including UTRs) Position: hg38 chr10:80,150,889-80,205,572 Size: 54,684 Total Exon Count: 17 Strand: - Coding Region Position: hg38 chr10:80,155,853-80,172,861 Size: 17,009 Coding Exon Count: 14
ID:Q5T0G8_HUMAN DESCRIPTION: RecName: Full=Annexin; DOMAIN: A pair of annexin repeats may form one binding site for calcium and phospholipid (By similarity). SIMILARITY: Belongs to the annexin family. SIMILARITY: Contains 4 annexin repeats.
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 Q5T0G8
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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
