KEGG   VARIANT: 3371v1
Entry
3371v1                      Variant                                
Name
TNC mutation
Type
Loss of function
Gene
TNC  tenascin C [KO:K06252]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 187380
Network
nt06548  Integrin signaling
Disease
H00604  Deafness, autosomal dominant
Reference
  Authors
Zhao Y, Zhao F, Zong L, Zhang P, Guan L, Zhang J, Wang D, Wang J, Chai W, Lan L, Li Q, Han B, Yang L, Jin X, Yang W, Hu X, Wang X, Li N, Li Y, Petit C, Wang J, Wang HY, Wang Q
  Title
Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss.
  Journal
PLoS One 8:e69549 (2013)
DOI:10.1371/journal.pone.0069549
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