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Repository for lectin-assisted multimodality data
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MIRAGE
cadherin 11
Summary
- Gene Symbol
-
- CDH11
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Calcium
- Cell adhesion
- Cell membrane
- Chromosomal rearrangement
- Cleavage on pair of basic residues
- Deafness
- Disease variant
- Glycoprotein
- Intellectual disability
- Metal-binding
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell morphogenesis | ||
| skeletal system development | ||
| ossification | ||
| aortic valve formation | ||
| cell-cell junction assembly |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region | ||
| cytoplasm | ||
| plasma membrane | ||
| adherens junction | ||
| catenin complex |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| calcium ion binding | ||
| beta-catenin binding | ||
| cadherin binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Cadherin
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
| InterPro |
|---|
| Cadherin conserved site |
| Cadherin, Y-type LIR-motif |
| Cadherin-like superfamily |
| Cadherin-like |
| Cadherin |
| Catenin binding domain superfamily |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080631 | Elsahy-Waters syndrome | |
| DOID:0081074 | Teebi hypertelorism syndrome 2 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101587366 | OCTDE03630 | ||
| 101613365 | JACJA15082 | ||
| 101678312 | MUSPF16912 | ||
| 101708158 | HETGA22645 | ||
| 101815280 | FICAL10093 | ||
| 101871801 | MELUD03435 | ||
| 101952849 | CHRPI21047 | ||
| 102019097 | CHILA09474 | ||
| 102173493 | CAPHI08583 | ||
| 102354463 | LATCH04713 |
