Gene

ceh-13

Species
Caenorhabditis elegans
Symbol
ceh-13
Name
C. Elegans Homeobox 13
Synonyms
  • CELE_R13A5.5
  • R13A5.5
Biotype
protein coding gene
Automated Description
Predicted to enable DNA-binding transcription factor activity. Involved in cell-cell adhesion and embryo development. Located in cytoplasm and nucleus. Is expressed in several structures, including embryonic cell; hypodermal cell; neurons; somatic nervous system; and in male. Human ortholog(s) of this gene implicated in Athabaskan brainstem dysgenesis syndrome and autistic disorder. Orthologous to several human genes including HOXB1 (homeobox B1) and HOXD1 (homeobox D1).
WB Description
a homolog of Hox genes of labial/Hox1 type; affects viability, body shape and anterior patterning during embryogenesis, interacts genetically with hox genes; and is expressed in A, D, E and MS lineages in the early embryo, and in the anterior dorsal hypodermal cells, anterior body wall muscle cells, and in the cells of the prospective ventral nerve cord at the comma stage; and in the ventral nerve cord and and ventral and dorsal hypodermal cells in L1 larvae.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR45946
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
None

Disease Associations

Cases where the expected disease association was NOT found
Cell color indicative of annotation volume

Transgenic Alleles

Models

Sequence Feature Viewer

Genome location
Assembly version
WBcel235
Viewer Help
7.5558M7.5560M7.5562M7.5564M7.5566M7.5568M7.5570M7.5572M7.5574M7.5576M7.5578M7.5580M

Sequence Details

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Expression

Primary Sources
Other Sources
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

Genetic Interactions