Version: 8.0.0Date: Tue Jan 28 2025
Gene
C11H1.7
- Species
- Caenorhabditis elegans
- Symbol
- C11H1.7
- Name
- DUF3456 domain-containing protein
- Synonyms
- CELE_C11H1.7
- Biotype
- protein coding gene
- Automated Description
- Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 60. Orthologous to several human genes including CNPY4 (canopy FGF signaling regulator 4).
- WB Description
- Predicted to enable signaling receptor binding activity. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 60. Is an ortholog of human CNPY4 (canopy FGF signaling regulator 4).
- Cross References
- Additional Information
- Literature
Orthology
- Gene tree
- PANTHER:PTHR15382
Stringency:
Additional filters to further constrain the results:
| Species | Gene symbol | Count | Best | Best reverse | Method Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN |
|---|---|---|---|---|---|
| Homo sapiens | CNPY4 | 7 of 9 | Yes | Yes | ☑ ☑☑☐☑☑☑☐☑ |
| Homo sapiens | CNPY3 | 6 of 9 | No | Yes | ☑ ☐☑☐☑☑☑☐☑ |
| Mus musculus | Cnpy3 | 7 of 9 | Yes | Yes | ☑ ☐☑☐☑☑☑☑☑ |
| Mus musculus | Cnpy4 | 7 of 9 | Yes | Yes | ☑ ☑☑☐☑☑☑☐☑ |
| Rattus norvegicus | Cnpy3 | 7 of 9 | Yes | Yes | ☑ ☐☑☐☑☑☑☑☑ |
| Rattus norvegicus | Cnpy4 | 7 of 9 | Yes | Yes | ☑ ☑☑☐☑☑☑☐☑ |
| Danio rerio | cnpy4 | 8 of 9 | Yes | Yes | ☑ ☑☑☑☑☑☑☐☑ |
| Danio rerio | cnpy3 | 7 of 9 | No | Yes | ☑ ☐☑☐☑☑☑☑☑ |
| Drosophila melanogaster | CNPYb | 8 of 9 | Yes | Yes | ☑ ☑☑☐☑☑☑☑☑ |
Links to orthology data in JBrowse by filter level: Stringent, Moderate, No filter, Best and Best Reverse
Disease Associations
Cases where the expected disease association was NOT found
| all annotations | all disease by infectious agent | bacterial infectious disease | fungal infectious disease | parasitic infectious disease | viral infectious disease | all disease of anatomical entity | cardiovascular system disease | central nervous system disease | endocrine system disease | gastrointestinal system disease | hematopoietic system disease | immune system disease | integumentary system disease | musculoskeletal system disease | peripheral nervous system disease | reproductive system disease | respiratory system disease | sensory system disease | thoracic disease | urinary system disease | all disease of cellular proliferation | benign neoplasm | cancer | pre-malignant neoplasm | all genetic disease | chromosomal disease | monogenic disease | polygenic disease | all other disease | disease of mental health | disease of metabolism | physical disorder | syndrome | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C11H1.7 (Cel) |
Cell color indicative of annotation volume
No data available
Alleles and Variants
- Genome location
- ChrX:14327409...14330195 + (2.79 kb)
- Assembly version
- WBcel235
- Viewer Help
Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.
Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
|---|---|---|---|---|---|---|---|
| NC_003284.9:g.14327568C>T | variant | SNP
| |||||
| NC_003284.9:g.14328087C>T | variant | SNP
| |||||
| NC_003284.9:g.14328601G>A | variant | SNP
| |||||
| NC_003284.9:g.14328837T>G | variant | SNP
| |||||
| NC_003284.9:g.14327445T>A | variant | SNP
| |||||
| NC_003284.9:g.14329200T>G | variant | SNP
| |||||
| NC_003284.9:g.14328848T>A | variant | SNP
| |||||
| NC_003284.9:g.14328326A>T | variant | SNP
| |||||
| NC_003284.9:g.14328068G>A | variant | SNP
| |||||
| NC_003284.9:g.14328166C>G | variant | SNP
| |||||
Sequence Feature Viewer
- Genome location
- ChrX:14327409...14330195 + (2.79 kb)
- Assembly version
- WBcel235
- Viewer Help
Expression
- Primary Sources
- Other Sources
| all annotations | all anatomical structures | alimentary part of gastrointestinal system | chemosensory system | circulatory system | endocrine system | exocrine system | hemolymphoid system | hepatobiliary system | integumental system | mechanosensory system | musculoskeletal system | nervous system | renal system | reproductive system | respiratory system | sensory system | vestibulo-auditory system | visual system | endoderm | ectoderm | mesoderm | mesenchyme | adipose tissue | appendage | entire extraembryonic component | imaginal precursor | pharyngeal arch | other | all stages | embryo stage | post embryonic, pre-adult | post-juvenile adult stage | all cellular components | extracellular region | plasma membrane | synapse | cell junction | cell projection | cytoplasmic vesicle | endosome | vacuole | golgi apparatus | endoplasmic reticulum | cytosol | mitochondrion | nucleus | chromosome | cytoskeleton | protein-containing complex | other locations | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| C11H1.7 (Cel) |
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.