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
Resources Genes Glycoproteins Lectins Glycolipids Glycans Pathways Diseases Organisms
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Other Information
Release Statistics Download
Tools
SugarDrawer GlycanBuilder Glycan Converters GlycoMaple GlycomeAtlas LM-GlycomeAtlas GALAXY MCAW GlycoSim GRable
Search Tools
Cross Search Glycan Search Publication Search Programmatic Access
Standards Ontologies Notations
Guidelines
MIRAGE
tectorin alpha

Summary
Gene Symbol
  • TECTA
Organism
Homo sapiens (human)
NCBI Gene
7007
HGNC
11720
KEGG Gene ID
PubChem
7007
Alliance of Genome Resources
JoGo
TECTA
TogoVar
TECTA
Annotation
Keyword
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Extracellular matrix
  • GPI-anchor
  • Hearing
  • Non-syndromic deafness
  • Reference proteome
  • Repeat
  • Signal
Proteins
Displaying 1 entry
UniProt Protein Name
O75443
Annotation information from UniProt.
Gene Ontology (GO)
Gene Ontology information from NCBI Gene and UniProt.
KEGG BRITE Database
Orthology
K18273
Name
alpha-tectorin
References
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0110544 autosomal dominant nonsyndromic deafness 12
DOID:0110479 autosomal recessive nonsyndromic deafness 21
DOID:10003 sensorineural hearing loss
The Human Phenotype Ontology
Displaying all 3 entries
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000007 Autosomal recessive inheritance
HP:0000407 Sensorineural hearing impairment
Displaying all 2 entries
Disease ID Disease Name
OMIM:603629
  • autosomal recessive nonsyndromic hearing loss 21
OMIM:601543
  • autosomal dominant nonsyndromic hearing loss 12
PubChem Disease
GHR Health Conditions
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
Ortholog
Displaying 1 entry
Species Gene ID Alliance of Genome Resources
21683 MGI:109575
About Release Notes Help Feedback
International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

Logo License Policies Site Map

Contact: [email protected]

This work is licensed under Creative Commons Attribution 4.0 International

GlyCosmos Portal v4.5.0

Last updated: April 6, 2026