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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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TECTB
tectorin beta
Chromosome 10 · 10q25.2
NCBI Gene: 6975Ensembl: ENSG00000119913.6HGNC: HGNC:11721UniProt: Q96PL2
11PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
extracellular matrix structural constituentGO:0005615cell surfaceextracellular regionliver diseasecirrhosis of liveralcohol drinkingaortic disease
✦AI Summary

TECTB (tectorin beta) is a major non-collagenous structural component of the tectorial membrane (TM), a specialized extracellular matrix overlying the cochlear sensory epithelium 1. The TM is essential for sound transduction, as sound-induced hair cell movement relative to the TM deflects stereocilia bundles and generates electrical signals [UniProt]. TECTB contains a zona pellucida (ZP) domain with eight conserved cysteines critical for proper protein folding and matrix assembly 1. The protein functions primarily in TM structural integrity; TECTB interacts with alpha-tectorin (TECTA) and other matrix proteins to form the striated-sheet matrix that embeds collagen fibrils 2. TECTB is essential for normal hearing development, as mutations cause hearing loss through disrupted TM morphology. A missense variant (p.Cys225Tyr) causes autosomal dominant non-syndromic hearing loss, with homozygous animals exhibiting severe hearing loss and TM disorganization, while heterozygotes show increased susceptibility to noise-induced hearing loss 1. Additionally, TECTB levels are regulated by hepsin-mediated proteolytic processing during TM development 3. TECTB is transcriptionally downregulated in blood associated with comorbid psychopathology, though the neurobiological significance remains unclear 4.

Sources cited
1
TECTB missense variant (p.Cys225Tyr) causes autosomal dominant hearing loss; contains conserved cysteines in ZP domain critical for folding and matrix assembly; homozygous mice exhibit severe hearing loss and TM disruption; heterozygotes show reduced TM matrix content and increased noise-induced hearing loss susceptibility
PMID: 40832383
2
TECTB is a non-collagenous protein crucial for TM formation; hepsin regulates TECTB levels through proteolytic processing/maturation; decreased TECTB levels in hepsin knockout mice; TECTB co-expressed with TECTA in developing cochlear epithelium
PMID: 39437584
3
TECTB is a secreted glycoprotein present in tectorial membrane; required for striated-sheet matrix formation embedding collagen fibrils; interacts with TECTA and CEACAM16
PMID: 25080593
4
Mutations in genes encoding α- and β-tectorin reveal multiple roles for the tectorial membrane in stimulating hair bundles
PMID: 21073336
5
TECTB is deficient in tectorial membrane when TECTA function is impaired; required for proper TM matrix organization
PMID: 18452040
6
TECTB downregulation in blood is associated with comorbid psychopathology in depressive disorders
PMID: 40672507
7
Beta-tectorin is inner ear-specific protein that can elicit CD4+ T cell-mediated autoimmune sensorineural hearing loss
PMID: 15085190
Disease Associationsⓘ20
liver diseaseOpen Targets
0.44Moderate
cirrhosis of liverOpen Targets
0.33Weak
alcohol drinkingOpen Targets
0.32Weak
aortic diseaseOpen Targets
0.31Weak
metabolic syndromeOpen Targets
0.31Weak
neurodegenerative diseaseOpen Targets
0.25Weak
deafnessOpen Targets
0.08Suggestive
hearing loss, autosomal recessiveOpen Targets
0.08Suggestive
autosomal dominant nonsyndromic hearing lossOpen Targets
0.07Suggestive
hearing loss, autosomal dominant 85Open Targets
0.05Suggestive
hearing loss, autosomal dominant 86Open Targets
0.05Suggestive
hearing loss, autosomal dominant 87Open Targets
0.05Suggestive
X-linked nonsyndromic hearing lossOpen Targets
0.05Suggestive
hearing loss, autosomal dominant 75Open Targets
0.05Suggestive
hearing loss, autosomal dominant 77Open Targets
0.05Suggestive
hearing loss, autosomal recessive 118, with cochlear aplasiaOpen Targets
0.05Suggestive
EpiphoraOpen Targets
0.05Suggestive
Non-syndromic genetic deafnessOpen Targets
0.05Suggestive
Autosomal recessive cerebellar ataxia - blindness - deafnessOpen Targets
0.05Suggestive
peroxisome biogenesis disorder 4BOpen Targets
0.05Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
OTOGProtein interaction97%OTOAProtein interaction96%OTOGLProtein interaction90%COCHProtein interaction90%ZANProtein interaction84%NID1Protein interaction74%
Tissue Expression6 tissues
Liver
100%
Brain
11%
Bone Marrow
2%
Lung
0%
Heart
0%
Ovary
0%
Gene Interaction Network
Click a node to explore
TECTBOTOGOTOAOTOGLCOCHZANNID1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q96PL2
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.26LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.97 [0.76–1.26]
RankingsWhere TECTB stands among ~20K protein-coding genes
  • #16,917of 20,598
    Most Researched11
  • #13,255of 17,882
    Most Constrained (LOEUF)1.26
Genes detectedTECTB
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Critical role of hepsin/TMPRSS1 in hearing and tectorial membrane morphogenesis: Insights from transgenic mouse models.
PMID: 39437584
Hear Res · 2024
1.00
2
The
PMID: 40832383
medRxiv · 2025
0.90
3
[In silicon cloning of the human TECTB gene].
PMID: 12812054
Yi Chuan Xue Bao · 2003
0.80
4
Loss of the tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions.
PMID: 25080593
J Neurosci · 2014
0.70
5
Brain network and blood transcriptomic correlations underpin psychopathological phenotypes: A Preliminary Study.
PMID: 40672507
medRxiv · 2025
0.60