Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 259236
MIM: 607237
HGNC: 30800
Ensembl: ENSG00000181585
Variants:
dbSNP: 259236
ClinVar: 259236
TCGA: ENSG00000181585
COSMIC: TMIE
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000181585 | ENST00000643606 | Q8NEW7 |
| ENSG00000181585 | ENST00000644830 | A0A2R8YDZ8 |
| ENSG00000181585 | ENST00000651652 | A0A494C1A3 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35710363 | 2022 | Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness. | 1 |
| 35710363 | 2022 | Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness. | 1 |
| 24416283 | 2014 | Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE. | 28 |
| 24416283 | 2014 | Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE. | 28 |
| 20206386 | 2010 | Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss. | 7 |
| 20206386 | 2010 | Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss. | 7 |
| 20206386 | 2010 | Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss. | 7 |
| 20206386 | 2010 | Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss. | 7 |
| 19438934 | 2009 | A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia. | 10 |
| 19438934 | 2009 | A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia. | 10 |
| 14727813 | 2003 | Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9. | 7 |
| 14727813 | 2003 | Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9. | 7 |
| 12140191 | 2002 | Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6. | 50 |
| 12145746 | 2002 | Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus. | 58 |
| 12140191 | 2002 | Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6. | 50 |
Citation
Dessen P
TMIE (transmembrane inner ear)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/74999/tmie-(transmembrane-inner-ear)
