| 1 | CEACAM16, DFNB113
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| A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss
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| Zhang D, Wu J, Yuan Y, Li X, Gao X, Han M, Gao S, Huang S, Dai P.
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| Ann Hum Genet. Jul;86(4):207-217. doi: 10.1111/ahg.12463. Epub 2022 Mar 16. 2022
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| 2 | CEACAM16
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| Comparing spontaneous and stimulus frequency otoacoustic emissions in mice with tectorial membrane defects.
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| Cheatham MA.
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| Hear Res. Feb;400:108143. doi: 10.1016/j.heares.2020.108143. Epub 2020 Dec 5. 2021
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| 3 | CEACAM16, DFNB113
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| Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans.
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| Dias AMM, Lezirovitz K, Nicastro FS, Mendes BCA, Mingroni-Netto RC.
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| Eur J Hum Genet. Mar;64(3):257-260. doi: 10.1038/s10038-018-0546-4. Epub 2018 Dec 4. 2019
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| 4 | CEACAM16, DFNB113
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| Old gene, new phenotype: splice-altering variants in CEACAM16 cause recessive non-syndromic hearing impairment.
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| Booth KT, Kahrizi K, Najmabadi H, Azaiez H, Smith RJ.
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| J Med Genet. Aug;55(8):555-560. doi: 10.1136/jmedgenet-2018-105349. Epub 2018 Apr 27 2018
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| 5 | CEACAM16, DFNA4B
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| Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.
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| Wang H, Wang X, He C, Li H, Qing J, Grati M, Hu Z, Li J, Hu Y, Xia K, Mei L, Wang X, Yu J, Chen H, Jiang L, Liu Y, Men M, Zhang H, Guan L, Xiao J, Zhang J, Liu X, Feng Y.
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| J Hum Genet 60(3):119-126. doi: 10.1038/jhg.2014.114. Epub 2015 Jan 15.
2015
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| 6 | CEACAM16, DFNA4B, DFNB113
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| A Novel de novo Mutation in CEACAM16 Associated with Postlingual Hearing Impairment.
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| Hofrichter MA, Nanda I, Gräf J, Schröder J, Shehata-Dieler W, Vona B, Haaf T.
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| Mol Syndromol. Oct;6(4):156-63. doi: 10.1159/000439576. Epub 2015 Sep 3. 2015
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| 7 | CEACAM16, TECTA, TECTB
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| Loss of the tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions.
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| Cheatham MA, Goodyear RJ, Homma K, Legan PK, Korchagina J, Naskar S, Siegel JH, Dallos P, Zheng J, Richardson GP.
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| J Neurosci 34(31):10325-38. doi: 10.1523/JNEUROSCI.1256-14.2014.
2014
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| 8 | CEACAM16
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| Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.
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| Kammerer R, Rüttiger L, Riesenberg R, Schäuble C, Krupar R, Kamp A, Sunami K, Eisenried A, Hennenberg M, Grunert F, Bress A, Battaglia S, Schrewe H, Knipper M, Schneider MR, Zimmermann W.
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| J Biol Chem 287(26):21584-98. doi: 10.1074/jbc.M111.320481. Epub 2012 Apr 27.
2012
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| 9 | CEACAM16, DFNA4B
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| Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).
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| Zheng J, Miller KK, Yang T, Hildebrand MS, Shearer AE, DeLuca AP, Scheetz TE, Drummond J, Scherer SE, Legan PK, Goodyear RJ, Richardson GP, Cheatham MA, Smith RJ, Dallos P.
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| Proc Natl Acad Sci U S A 108(10):4218-23. doi: 10.1073/pnas.1005842108. Epub 2011 Feb 22.
2011
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| 10 | CEACAM16, CEACAM18, CEACAM19, CEACAM21
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| Identification of a novel group of evolutionarily conserved members within the rapidly diverging murine Cea family.
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| Zebhauser R, Kammerer R, Eisenried A, McLellan A, Moore T, Zimmermann W.
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| Genomics 86(5):566-80. Epub 2005 Sep 1. 2005
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