Jump to content
Wikipedia The Free Encyclopedia

Dynein axonemal light chain 1

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
DNAL1
Identifiers
Aliases DNAL1 , C14orf168, CILD16, dynein axonemal light chain 1, LC1
External IDsOMIM: 610062; MGI: 1921462; HomoloGene: 34623; GeneCards: DNAL1; OMA:DNAL1 - orthologs
Gene location (Human)
Chromosome 14 (human)
Chr. Chromosome 14 (human) [1]
Band 14q24.3Start73,644,875 bp [1]
End73,703,732 bp [1]
Gene location (Mouse)
Chromosome 12 (mouse)
Chr. Chromosome 12 (mouse)[2]
Band 12|12 D1Start84,161,140 bp [2]
End84,194,272 bp [2]
RNA expression pattern
Bgee
Human Mouse (ortholog)
  • buccal mucosa cell

  • left testis

  • right testis

  • bronchial epithelial cell

  • mucosa of paranasal sinus

  • Achilles tendon

  • corpus callosum

  • caput epididymis

  • islet of Langerhans

  • internal globus pallidus
  • otolith organ

  • utricle

  • Region I of hippocampus proper

  • nucleus accumbens

  • temporal lobe

  • lateral septal nucleus

  • amygdala

  • dorsal striatum

  • piriform cortex

  • prefrontal cortex
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

83544

105000

Ensembl

ENSG00000119661

ENSMUSG00000042523

UniProt

Q4LDG9

Q05A62

RefSeq (mRNA)

NM_001201366
NM_031427

NM_028821
NM_001346528

RefSeq (protein)

NP_001188295
NP_113615

NP_001333457
NP_083097

Location (UCSC)Chr 14: 73.64 – 73.7 Mb Chr 12: 84.16 – 84.19 Mb
PubMed search[3] [4]
Wikidata

Dynein axonemal light chain 1, (LC1) is a protein that in humans is encoded by the DNAL1 gene.[5] [6]

Function

[edit ]

LC1 is a component of outer dynein arms, which contain the molecular motors for ATP-dependent cilia movement.[5] [6]

Clinical significance

[edit ]

Mutations in the DNAL1 gene are associated with primary ciliary dyskinesia.[7]

References

[edit ]
  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000119661 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000042523 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.
  5. 1 2 "Entrez Gene: dynein".
  6. 1 2 Horváth J, Fliegauf M, Olbrich H, Kispert A, King SM, Mitchison H, Zariwala MA, Knowles MR, Sudbrak R, Fekete G, Neesen J, Reinhardt R, Omran H (July 2005). "Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients" . Am. J. Respir. Cell Mol. Biol. 33 (1): 41–7. doi:10.1165/rcmb.2004-0335OC. PMID 15845866. S2CID 19776274.
  7. Lancaster MA, Gleeson JG (June 2009). "The primary cilium as a cellular signaling center: lessons from disease". Curr. Opin. Genet. Dev. 19 (3): 220–9. doi:10.1016/j.gde.200904008. PMC 2953615 . PMID 19477114.
[edit ]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Stub icon

This article on a gene on human chromosome 14 is a stub. You can help Wikipedia by adding missing information.

AltStyle によって変換されたページ (->オリジナル) /