- DNAH11
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Dynein, axonemal, heavy chain 11 Identifiers Symbols DNAH11; CILD7; DNAHBL; DNAHC11; DNHBL; DPL11; FLJ30095; FLJ37699 External IDs OMIM: 603339 MGI: 1100864 HomoloGene: 2801 GeneCards: DNAH11 Gene Gene Ontology Molecular function • nucleotide binding
• microtubule motor activity
• ATP binding
• ATPase activityCellular component • cytoplasm
• cytoskeleton
• axonemal dynein complex
• microtubule
• cilium
• cilium axonemeBiological process • microtubule-based movement Sources: Amigo / QuickGO RNA expression pattern 
More reference expression data Orthologs Species Human Mouse Entrez 8701 13411 Ensembl ENSG00000105877 ENSMUSG00000018581 UniProt Q96DT5 n/a RefSeq (mRNA) NM_003777 NM_010060.2 RefSeq (protein) NP_003768 NP_034190.2 Location (UCSC) Chr 7:
21.58 – 21.94 MbChr 12:
119.12 – 119.44 MbPubMed search [1] [2] Dynein heavy chain 11, axonemal is a protein that in humans is encoded by the DNAH11 gene.[1][2]
Contents
Function
This gene encodes a member of the dynein heavy chain family. It is a microtubule-dependent motor ATPase and has been reported to be involved in the movement of respiratory cilia. Mutations in this gene have been implicated in causing primary ciliary dyskinesia (PCD, formerly called 'immotile cilia syndrome') and Kartagener syndrome (PCD with situs inversus totalis). Males with PCD are not sterile, but are infertile due to lack of sperm motility.[2]. There are reports of subfertility and increased risk of ectopic pregnancy in women with PCD. [3]
References
- ^ Chapelin C, Duriez B, Magnino F, Goossens M, Escudier E, Amselem S (Sep 1997). "Isolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment". FEBS Lett 412 (2): 325–30. doi:10.1016/S0014-5793(97)00800-4. PMID 9256245.
- ^ a b "Entrez Gene: DNAH11 dynein, axonemal, heavy chain 11". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8701.
- ^ Blyth M, Wellesley D (April 2008). "Ectopic pregnancy in primary ciliary dyskinesia". J Obstet Gynaecol 28 (3): 358. doi:10.1080/01443610802058742. PMID 18569496.
Further reading
- Schwabe GC, Hoffmann K, Loges NT, et al. (2008). "Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations.". Hum. Mutat. 29 (2): 289–98. doi:10.1002/humu.20656. PMID 18022865.
- Cheung PY, Zhang Y, Long J, et al. (2004). "p150(Glued), Dynein, and microtubules are specifically required for activation of MKK3/6 and p38 MAPKs.". J. Biol. Chem. 279 (44): 45308–11. doi:10.1074/jbc.C400333200. PMID 15375157.
- Varadi A, Johnson-Cadwell LI, Cirulli V, et al. (2005). "Cytoplasmic dynein regulates the subcellular distribution of mitochondria by controlling the recruitment of the fission factor dynamin-related protein-1.". J. Cell. Sci. 117 (Pt 19): 4389–400. doi:10.1242/jcs.01299. PMID 15304525.
- 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.
- Hillier LW, Fulton RS, Fulton LA, et al. (2003). "The DNA sequence of human chromosome 7.". Nature 424 (6945): 157–64. doi:10.1038/nature01782. PMID 12853948.
- Bartoloni L, Blouin JL, Pan Y, et al. (2002). "Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia.". Proc. Natl. Acad. Sci. U.S.A. 99 (16): 10282–6. doi:10.1073/pnas.152337699. PMC 124905. PMID 12142464. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=124905.
- Dias Neto E, Correa RG, Verjovski-Almeida S, et al. (2000). "Shotgun sequencing of the human transcriptome with ORF expressed sequence tags.". Proc. Natl. Acad. Sci. U.S.A. 97 (7): 3491–6. doi:10.1073/pnas.97.7.3491. PMC 16267. PMID 10737800. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=16267.
- Kastury K, Taylor WE, Gutierrez M, et al. (1997). "Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11.". Genomics 44 (3): 362–4. doi:10.1006/geno.1997.4903. PMID 9325061.
External links
Categories:- Human proteins
- Protein stubs
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