======= TMIE =======
== Gene Information ==
* **Official Symbol**: TMIE
* **Official Name**: transmembrane inner ear
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=259236|259236]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q8NEW7|Q8NEW7]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=TMIE&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20TMIE|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/607237|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment. [provided by RefSeq, Mar 2009].
* **UniProt Summary**: Unknown. The protein may play some role in a cellular membrane location. May reside within an internal membrane compartment and function in pathways such as those involved in protein and/or vesicle trafficking. Alternatively, the mature protein may be localized in the plasma membrane and serve as a site of interaction for other molecules through its highly charged C-terminal domain.
No Pfam Domain information is available for this gene.
|inner ear morphogenesis|
|ear morphogenesis|
|sensory perception of sound|
|sensory perception of mechanical stimulus|
|inner ear development|
|ear development|
|sensory organ morphogenesis|
|embryonic organ morphogenesis|
|embryonic organ development|
|sensory organ development|
|embryonic morphogenesis|
|animal organ morphogenesis|
|sensory perception|
|embryo development|
|nervous system process|
|system process|
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp314|Dimethyloxaloylglycine 11μM R07 exp314]]|-1.98|
|[[:results:exp269|Bisphenol A 100μM R06 exp269]]|1.72|
|[[:results:exp456|Benzoate 20000μM R08 exp456]]|1.89|
|[[:results:exp299|Talazoparib 0.006μM R06 exp299]]|1.89|
No correlation found to any other genes in chemogenomics.
Global Fraction of Cell Lines Where Essential: 0/739
^Tissue^Fraction Of Cell Lines Where Essential^
|1290807.0|0/1|
|909776.0|0/1|
|bile duct|0/28|
|blood|0/28|
|bone|0/26|
|breast|0/33|
|central nervous system|0/56|
|cervix|0/4|
|colorectal|0/17|
|esophagus|0/13|
|fibroblast|0/1|
|gastric|0/16|
|kidney|0/21|
|liver|0/20|
|lung|0/75|
|lymphocyte|0/16|
|ovary|0/26|
|pancreas|0/24|
|peripheral nervous system|0/16|
|plasma cell|0/15|
|prostate|0/1|
|skin|0/24|
|soft tissue|0/9|
|thyroid|0/2|
|upper aerodigestive|0/22|
|urinary tract|0/29|
|uterus|0/5|
== Essentiality in NALM6 ==
* **Essentiality Rank**: 13328
* **Expression level (log2 read counts)**: 3.33
{{:chemogenomics:nalm6 dist.png?nolink |}}