Human Gene FOXD4L1 (ENST00000306507.7) from GENCODE V44
Description: Homo sapiens forkhead box D4 like 1 (FOXD4L1), mRNA. (from RefSeq NM_012184) RefSeq Summary (NM_012184): This gene is a member of the forkhead/winged-helix (FOX) family of transcription factors with highly conserved FOX DNA-binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily in subtelomeric and pericentromeric locations, thus mutiple copies of this gene have been found. [provided by RefSeq, Jul 2008]. Gencode Transcript: ENST00000306507.7 Gencode Gene: ENSG00000184492.7 Transcript (Including UTRs) Position: hg38 chr2:113,498,665-113,501,150 Size: 2,486 Total Exon Count: 1 Strand: + Coding Region Position: hg38 chr2:113,499,257-113,500,483 Size: 1,227 Coding Exon Count: 1
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 Q9NU39
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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
