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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
orofacial cleft
Summary
- Definition
- A physical disorder that is characterized by cleft lip and/or cleft palate that result in feeding, speech and hearing problems caused by failures during development.
- Super Class
- physical disorder syndrome
External Links
- Disease Ontology
- DOID:0050567
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 4627 | MYH9 | myosin heavy chain 9 | |
| 23384 | SPECC1L | sperm antigen with calponin homology and coiled-coil domains 1 like | |
| 55902 | ACSS2 | acyl-CoA synthetase short chain family member 2 | |
| 83716 | CRISPLD2 | cysteine rich secretory protein LCCL domain containing 2 | |
| 125336 | LOXHD1 | lipoxygenase homology PLAT domains 1 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 17886 | Myh9 | myosin, heavy polypeptide 9, non-muscle | |
| 74392 | Specc1l | sperm antigen with calponin homology and coiled-coil domains 1-like | |
| 78892 | Crispld2 | cysteine-rich secretory protein LCCL domain containing 2 | |
| 240411 | Loxhd1 | lipoxygenase homology domains 1 |
