TBCEL-TECTA (TBCEL-TECTA readthrough)

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Gene Gene information from NCBI Gene database.
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Entrez ID 116804918
Gene name TBCEL-TECTA readthrough
Gene symbol TBCEL-TECTA
Synonyms (NCBI Gene)
-
Chromosome 11
Chromosome location 11q23.3
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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MIM HGNC e!Ensembl
HGNC 54857 N/A
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
11
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Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Show/Hide Unknown Diseases (11)
Phenotype Name Clinical Significance Source Reference Evidence Score
AUTOIMMUNE DISORDER OF MUSCULOSKELETAL SYSTEM — GWAS catalog 39024449
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL EAR ANOMALY NOS — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL SENSORINEURAL HEARING LOSS — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEAFNESS, AUTOSOMAL DOMINANT 12 — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEAFNESS, AUTOSOMAL RECESSIVE — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
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TECTA 5 shared diseasesNonsyndromic hearing loss, Congenital ear anomaly, Congenital sensorineural hearing loss, Deafness, Meniere disease 6 shared evidence sourcesDisgenet (Nonsyndromic hearing loss), Disgenet (Congenital ear anomaly), Disgenet (Congenital sensorineural hearing loss), Disgenet (Deafness), Disgenet (Hearing loss), Disgenet (Meniere disease) Related via 5 shared diseases including Nonsyndromic hearing loss, Congenital ear anomaly — evidence mostly Disgenet. C10orf105 3 shared diseasesCongenital ear anomaly, Deafness, Meniere disease 5 shared evidence sourcesDisgenet (Congenital ear anomaly), Disgenet (Deafness), Disgenet (Hearing loss), GWAS catalog (Hearing loss), Disgenet (Meniere disease) Related via 3 shared diseases including Congenital ear anomaly, Deafness — evidence mostly Disgenet. CEACAM16 3 shared diseasesNonsyndromic hearing loss, Congenital ear anomaly, Deafness 5 shared evidence sourcesDisgenet (Nonsyndromic hearing loss), Disgenet (Congenital ear anomaly), Disgenet (Deafness), Disgenet (Hearing loss), GWAS catalog (Hearing loss) Related via 3 shared diseases including Nonsyndromic hearing loss, Congenital ear anomaly — evidence mostly Disgenet. OTOG 3 shared diseasesNonsyndromic hearing loss, Deafness, Meniere disease 5 shared evidence sourcesDisgenet (Nonsyndromic hearing loss), Disgenet (Deafness), Disgenet (Hearing loss), GWAS catalog (Hearing loss), Disgenet (Meniere disease) Related via 3 shared diseases including Nonsyndromic hearing loss, Deafness — evidence mostly Disgenet. ILDR1 3 shared diseasesNonsyndromic hearing loss, Congenital sensorineural hearing loss, Deafness 5 shared evidence sourcesDisgenet (Nonsyndromic hearing loss), Disgenet (Congenital sensorineural hearing loss), Disgenet (Deafness), Disgenet (Hearing loss), GWAS catalog (Hearing loss) Related via 3 shared diseases including Nonsyndromic hearing loss, Congenital sensorineural hearing loss — evidence mostly Disgenet.
Isolated sensorineural deafness Linked via 4 of 5 related genesTECTA, CEACAM16, OTOG, ILDR1 nonsyndromic genetic hearing loss Linked via 4 of 5 related genesTECTA, CEACAM16, OTOG, ILDR1 Alzheimer disease Linked via 2 of 5 related genesTECTA, CEACAM16 Asthma Linked via 2 of 5 related genesOTOG, ILDR1 Esophageal disease Linked via 1 of 5 related genesTECTA