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  1. 1
    Cited for: NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY, VARIANTS DFNB6 CYS-81; TRP-84 AND TRP-92.
    Category: Pathology & Biotech, Expression, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  2. 2
    "Complete sequencing and characterization of 21,243 full-length human cDNAs."
    Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.
    , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
    Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
    Category: Sequences.
    Tissue: Amygdala.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 12929 other entries.

  3. 3
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  4. 4
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50488 other entries.

  5. 5
    "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."
    Mitchem K.L., Hibbard E., Beyer L.A., Bosom K., Dootz G.A., Dolan D.F., Johnson K.R., Raphael Y., Kohrman D.C.
    Hum. Mol. Genet. 11:1887-1898(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: genetic mapping data support human TMIE as the gene affected at DFNB6 a non-syndromic hearing loss locusImported.
    Source: GeneRIF:259236.

    This publication is cited by 2 and mapped to 48 other entries.

  6. 6
    "Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9."
    Cho K.I., Lee J.W., Kim K.S., Lee E.J., Suh J.G., Lee H.J., Kim H.T., Hong S.H., Chung W.H., Chang K.T., Hyun B.H., Oh Y.S., Ryoo Z.Y.
    Comp. Med. 53:642-648(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: The circling mouse is a potential animal model for DFNB6 deafness in humans.Imported.
    Source: GeneRIF:259236.

    This publication is mapped to 46 other entries.

  7. 7
    "A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia."
    Sirmaci A., Ozturkmen-Akay H., Erbek S., Incesulu A., Duman D., Tasir-Yilmaz S., Ozdag H., Tekin M.
    Clin. Genet. 75:562-567(2009) [PubMed] [Europe PMC] [Abstract]
    Annotation: p.R84W could be a common mutation in other Middle Eastern populations and should be included in mutation screening offered to individuals with autosomal recessive non-syndromic sensorineural hearing loss (ARNSSNHL)Imported.
    Source: GeneRIF:259236.
  8. 8
    "Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss."
    Yang J.J., Su M.C., Chien K.H., Hsin C.H., Li S.Y.
    Int. J. Pediatr. Otorhinolaryngol. 74:489-493(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: We suggest that a missense variant and one promoter variant is de novo and may be a risk factor for the development of hearing loss in Taiwanese; Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:259236.
  9. 9
    "Non-syndromic hearing impairment in India: high allelic heterogeneity among mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE."
    Ganapathy A., Pandey N., Srisailapathy C.R., Jalvi R., Malhotra V., Venkatappa M., Chatterjee A., Sharma M., Santhanam R., Chadha S., Ramesh A., Agarwal A.K., Rangasayee R.R., Anand A.
    PLoS ONE 9:e84773-e84773(2014) [PubMed] [Europe PMC] [Abstract]
    Annotation: Description of the spectrum of mutations in TMIE in 374 families with autosomal recessive non-syndromic hearing loss from India.Imported.
    Source: GeneRIF:259236.

    This publication is mapped to 21 other entries.

1 to 9 of 9  Show
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