TMPRSS3

TMPRSS3
Identifiers
Aliases	TMPRSS3 , DFNB10, DFNB8, ECHOS1, TADG12, transmembrane protease, serine 3, transmembrane serine protease 3
External IDs	OMIM: 605511 MGI: 2155445 HomoloGene: 56985 GeneCards: TMPRSS3
Gene location (Human)
Chr.	Chromosome 21 (human)
End	42,396,091 bp
Gene location (Mouse)
Chr.	Chromosome 17 (mouse)
End	31,417,951 bp
RNA expression pattern
	Top expressed in
	pancreatic ductal cell; ; right uterine tube; ; bronchial epithelial cell; ; pylorus; ; gallbladder; ; germinal epithelium; ; parotid gland; ; cardia; ; body of pancreas; ; lactiferous duct;
	Top expressed in
	utricle; ; cochlea; ; submandibular gland; ; parasympathetic nervous system; ; thyroid gland; ; pharynx; ; tongue; ; stria vascularis; ; bone marrow; ; saccule;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	scavenger receptor activity ; sodium channel regulator activity ; peptidase activity ; serine-type peptidase activity ; hydrolase activity ; serine-type endopeptidase activity ;
Cellular component	integral component of membrane ; neuronal cell body ; endoplasmic reticulum membrane ; endoplasmic reticulum ; membrane ;
Biological process	cellular sodium ion homeostasis ; sensory perception of sound ; receptor-mediated endocytosis ; proteolysis ; regulation of molecular function ; vesicle-mediated transport ; endocytosis ;
	Sources:Amigo / QuickGO
Orthologs
	64699
	140765
	ENSG00000160183
	ENSMUSG00000024034
	P57727
	Q8K1T0
	NM_001256317 ; NM_024022 ; NM_032401 ; NM_032404 ; NM_032405 Contents Function ; See also ; References ; Further reading ;
	NM_001163776 ; NM_080727
	NP_001243246 ; NP_076927 ; NP_115780 ; NP_115781
	NP_001157248 ; NP_542765
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated October 19, 2023

Transmembrane protease, serine 3 is an enzyme that in humans is encoded by the TMPRSS3 gene.^[5]^[6]^[7]

Function

This gene encodes a member of the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, an LDL receptor class A domain, and a scavenger receptor cysteine-rich domain. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified by its association with both congenital and childhood onset autosomal recessive deafness. This gene is expressed in fetal cochlea and many other tissues, and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph. This gene was also identified as a tumor associated gene that is overexpressed in ovarian tumors. Four alternatively spliced variants have been described, two of which encode identical products.^[7]

Related Research Articles

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Coiled-coil and C2 domain-containing protein 2A that in humans is encoded by the CC2D2A gene.

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Espin, also known as autosomal recessive deafness type 36 protein or ectoplasmic specialization protein, is a protein that in humans is encoded by the ESPN gene. Espin is a microfilament binding protein.

Forkhead box protein E3 (FOXE3) also known as forkhead-related transcription factor 8 (FREAC-8) is a protein that in humans is encoded by the FOXE3 gene located on the short arm of chromosome 1.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000160183 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000024034 - Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ Masmoudi S, Antonarakis SE, Schwede T, Ghorbel AM, Gratri M, Pappasavas MP, Drira M, Elgaied-Boulila A, Wattenhofer M, Rossier C, Scott HS, Ayadi H, Guipponi M (Jul 2001). "Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness". Hum Mutat. 18 (2): 101–8. doi: 10.1002/humu.1159 . PMID 11462234. S2CID 7917415.
↑ Wattenhofer M, Di Iorio MV, Rabionet R, Dougherty L, Pampanos A, Schwede T, Montserrat-Sentis B, Arbones ML, Iliades T, Pasquadibisceglie A, D'Amelio M, Alwan S, Rossier C, Dahl HH, Petersen MB, Estivill X, Gasparini P, Scott HS, Antonarakis SE (Mar 2002). "Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients". J Mol Med. 80 (2): 124–31. doi:10.1007/s00109-001-0310-6. PMID 11907649. S2CID 8185405.
1 2 "Entrez Gene: TMPRSS3 transmembrane protease, serine 3".

Guipponi M, Antonarakis SE, Scott HS (2007). "TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness". Front. Biosci. 13 (13): 1557–67. doi: 10.2741/2780 . PMID 17981648.
Bonné-Tamir B, DeStefano AL, Briggs CE, et al. (1996). "Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3". Am. J. Hum. Genet. 58 (6): 1254–9. PMC 1915077 . PMID 8651303.
Wallrapp C, Hähnel S, Müller-Pillasch F, et al. (2000). "A novel transmembrane serine protease (TMPRSS3) overexpressed in pancreatic cancer". Cancer Res. 60 (10): 2602–6. PMID 10825129.
Hattori M, Fujiyama A, Taylor TD, et al. (2000). "The DNA sequence of human chromosome 21". Nature. 405 (6784): 311–9. Bibcode:2000Natur.405..311H. doi: 10.1038/35012518 . PMID 10830953.
Underwood LJ, Shigemasa K, Tanimoto H, et al. (2001). "Ovarian tumor cells express a novel multi-domain cell surface serine protease". Biochim. Biophys. Acta. 1502 (3): 337–50. doi:10.1016/s0925-4439(00)00058-2. PMID 11068177.
Scott HS, Kudoh J, Wattenhofer M, et al. (2001). "Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness". Nat. Genet. 27 (1): 59–63. doi: 10.1038/83768 . PMID 11137999.
Ben-Yosef T, Wattenhofer M, Riazuddin S, et al. (2001). "Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness". J. Med. Genet. 38 (6): 396–400. doi:10.1136/jmg.38.6.396. PMC 1734898 . PMID 11424922.
Guipponi M, Vuagniaux G, Wattenhofer M, et al. (2003). "The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro" (PDF). Hum. Mol. Genet. 11 (23): 2829–36. doi:10.1093/hmg/11.23.2829. PMID 12393794.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi: 10.1073/pnas.242603899 . PMC 139241 . PMID 12477932.
Lee YJ, Park D, Kim SY, Park WJ (2003). "Pathogenic mutations but not polymorphisms in congenital and childhood onset autosomal recessive deafness disrupt the proteolytic activity of TMPRSS3". J. Med. Genet. 40 (8): 629–31. doi:10.1136/jmg.40.8.629. PMC 1735556 . PMID 12920079.
Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697 . PMID 12975309.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi: 10.1038/ng1285 . PMID 14702039.
Ahmed ZM, Li XC, Powell SD, et al. (2004). "Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan". BMC Med. Genet. 5: 24. doi:10.1186/1471-2350-5-24. PMC 523852 . PMID 15447792.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928 . PMID 15489334.
Wattenhofer M, Sahin-Calapoglu N, Andreasen D, et al. (2005). "A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein" (PDF). Hum. Genet. 117 (6): 528–35. doi:10.1007/s00439-005-1332-x. PMID 16021470. S2CID 27045077.
Stelzl U, Worm U, Lalowski M, et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome". Cell. 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. hdl: 11858/00-001M-0000-0010-8592-0 . PMID 16169070. S2CID 8235923.
Hu YH, Warnatz HJ, Vanhecke D, et al. (2006). "Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins". BMC Genomics. 7: 155. doi:10.1186/1471-2164-7-155. PMC 1526728 . PMID 16780588.
Elbracht M, Senderek J, Eggermann T, et al. (2007). "Autosomal recessive postlingual hearing loss (DFNB8): compound heterozygosity for two novel TMPRSS3 mutations in German siblings". J. Med. Genet. 44 (6): e81. doi:10.1136/jmg.2007.049122. PMC 2752172 . PMID 17551081.

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000160183 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000024034 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid11462234-5] Masmoudi S, Antonarakis SE, Schwede T, Ghorbel AM, Gratri M, Pappasavas MP, Drira M, Elgaied-Boulila A, Wattenhofer M, Rossier C, Scott HS, Ayadi H, Guipponi M (Jul 2001). "Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness". Hum Mutat. 18 (2): 101–8. doi: 10.1002/humu.1159 . PMID 11462234. S2CID 7917415.

[pmid11907649-6] Wattenhofer M, Di Iorio MV, Rabionet R, Dougherty L, Pampanos A, Schwede T, Montserrat-Sentis B, Arbones ML, Iliades T, Pasquadibisceglie A, D'Amelio M, Alwan S, Rossier C, Dahl HH, Petersen MB, Estivill X, Gasparini P, Scott HS, Antonarakis SE (Mar 2002). "Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients". J Mol Med. 80 (2): 124–31. doi:10.1007/s00109-001-0310-6. PMID 11907649. S2CID 8185405.

[entrez-7] 1 2 "Entrez Gene: TMPRSS3 transmembrane protease, serine 3".

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TMPRSS3

Contents

Function

See also

Related Research Articles

References

Further reading