Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
tectorin alpha
Summary
- Gene Symbol
-
- TECTA
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cell membrane
- Disease variant
- Disulfide bond
- Extracellular matrix
- GPI-anchor
- Hearing
- Non-syndromic deafness
- Reference proteome
- Repeat
- Signal
- Proteins
| UniProt | Protein Name |
|---|---|
| O75443 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| sensory perception of sound | ||
| cell-matrix adhesion | ||
| auditory receptor cell stereocilium organization |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular matrix | ||
| extracellular region |
|
|
| plasma membrane |
|
|
| side of membrane | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular matrix structural constituent |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110507 | autosomal recessive nonsyndromic deafness 5 | |
| DOID:0110508 | autosomal recessive nonsyndromic deafness 51 | |
| DOID:0110509 | autosomal recessive nonsyndromic deafness 53 | |
| DOID:0110510 | autosomal recessive nonsyndromic deafness 55 | |
| DOID:0110511 | autosomal recessive nonsyndromic deafness 59 | |
| DOID:0110512 | autosomal recessive nonsyndromic deafness 6 | |
| DOID:0110513 | autosomal recessive nonsyndromic deafness 61 | |
| DOID:0110514 | autosomal recessive nonsyndromic deafness 62 | |
| DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | |
| DOID:0110516 | autosomal recessive nonsyndromic deafness 65 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000407 | Sensorineural hearing impairment |
| Disease ID | Disease Name |
|---|---|
| OMIM:603629 |
|
| OMIM:601543 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 108696423 | Xenbase:XB-GENE-17333753 | ||
| 108697606 | Xenbase:XB-GENE-17333754 | ||
| 100490936 | Xenbase:XB-GENE-1011878 | ||
| 109317938 | CROPO23309 | ||
| 113441953 | PSETE14108 | ||
| 100538651 | MELGA08059 | ||
| 103823002 | SERCA19940 | ||
| 100913323 | SARHA02191 | ||
| 706506 | MACMU10108 | ||
| 712586 | MACMU10108 |
