Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
FRAS1 related extracellular matrix 1
Summary
- Gene Symbol
-
- FREM1
- Aliases
-
- C9orf143
- C9orf145
- DKFZp686M16108
- FLJ25461
- TILRR
- Organism
- Homo sapiens (human)
External Links
- NCBI Gene
- 158326
- HGNC
- 23399
- KEGG Gene ID
- hsa:158326
- PubChem
- 158326
- Alliance of Genome Resources
Annotation
- Keyword
-
- Alternative splicing
- Basement membrane
- Calcium
- Cell adhesion
- Craniosynostosis
- Developmental protein
- Disease variant
- Disulfide bond
- Glycoprotein
- Lectin
- Metal-binding
- Reference proteome
- Repeat
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| Q5H8C1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell-matrix adhesion | ||
| cell communication | ||
| anatomical structure morphogenesis | ||
| craniofacial suture morphogenesis |
| GO Term | Evidence Code | PMID |
|---|---|---|
| membrane | ||
| collagen-containing extracellular matrix | ||
| basement membrane | ||
| extracellular region |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| metal ion binding | ||
| carbohydrate binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- extracellular matrix
- Functional Category
-
- G: Carbohydrate transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| anatomical structure morphogenesis |
| cell communication |
| InterPro |
|---|
| CSPG repeat |
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060732 | chromosome 9p deletion syndrome | |
| DOID:0090001 | Fraser syndrome | |
| DOID:3827 | congenital diaphragmatic hernia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000316 | Hypertelorism |
| HP:0000322 | Short philtrum |
| HP:0000336 | Prominent supraorbital ridges |
| HP:0000358 | Posteriorly rotated ears |
| HP:0000369 | Low-set ears |
| HP:0000396 | Overfolded helix |
| HP:0000414 | Bulbous nose |
| HP:0000431 | Wide nasal bridge |
| HP:0000455 | Broad nasal tip |
| HP:0000456 | Bifid nasal tip |
| Disease ID | Disease Name |
|---|---|
| ORPHA:2717 |
|
| OMIM:248450 |
|
| OMIM:608980 |
|
| ORPHA:3366 |
|
| ORPHA:217266 |
|
| OMIM:614485 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 298185 | RGD:1306981 | RATNO34242 | ||
| 329872 | MGI:2670972 | MOUSE40729 | ||
| 464998 | 9598_0:0027e8 | PANTR43667 | ||
| 481547 | CANLF02183 | |||
| 508018 | BOVIN34311 | |||
| 557221 | ZFIN:ZDB-GENE-050208-783 | |||
| 713874 | MACMU12440 | |||
| 100020241 | MONDO30067 | |||
| 100062297 | HORSE21923 | |||
| 100172879 | 9601_0:00264f | PONAB35326 |
