Gene

Nme8

Species
Mus musculus
Symbol
Nme8
Name
NME/NM23 family member 8
Synonyms
  • 1700056P15Rik
  • RIKEN cDNA 1700056P15 gene
Biotype
protein coding gene
Automated Description
Predicted to enable 3'-5' exonuclease activity and microtubule binding activity. Acts upstream of or within cellular response to reactive oxygen species and flagellated sperm motility. Located in axoneme; sperm cytoplasmic droplet; and sperm principal piece. Human ortholog(s) of this gene implicated in primary ciliary dyskinesia 6. Orthologous to human NME8 (NME/NM23 family member 8).
MGI Description
PHENOTYPE: Homozygous mutant displays normal reproductive system phenotype [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR46135
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensNME810 of 10YesYes  
Rattus norvegicusNme89 of 9YesYes   
Xenopus tropicalisnme93 of 9YesYes   
Danio rerionme93 of 10YesNo  
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
Nme9142833233 of 9 
Nme7232648262 of 9 
Nme5313261393 of 9 
Nme4422436232 of 9 
Nme6513651302 of 9 
Nme3614748242 of 9 
Nme1713948252 of 9 
Nme2812950262 of 9 

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
No data available

Disease Associations

Cases where the expected disease association was NOT found
all annotationsall disease by infectious agentbacterial infectious diseasefungal infectious diseaseparasitic infectious diseaseviral infectious diseaseall disease of anatomical entitycardiovascular system diseasecentral nervous system diseaseendocrine system diseasegastrointestinal system diseasehematopoietic system diseaseimmune system diseaseintegumentary system diseasemusculoskeletal system diseaseperipheral nervous system diseasereproductive system diseaserespiratory system diseasesensory system diseasethoracic diseaseurinary system diseaseall disease of cellular proliferationbenign neoplasmcancerpre-malignant neoplasmall genetic diseasechromosomal diseasemonogenic diseasepolygenic diseaseall other diseasedisease of mental healthdisease of metabolismphysical disordersyndrome
Nme8 (Mmu)
Cell color indicative of annotation volume
No data available

Alleles and Variants

No mapped variant information available
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
Nme8tm1a(KOMP)Wtsiallele
Nme8em1(IMPC)Bayallele
Nme8em1Cya
  • Nme8em1
allele
Nme8em2Cya
  • Nme8em1flox
allele
Nme8tm1.1Arte
  • Sptrx-2-
allele
NC_000079.7:g.19833977A>Gvariant
SNP
  • intron variant
NC_000079.7:g.19840778G>Avariant
SNP
  • intron variant
NC_000079.7:g.19862783G>Avariant
SNP
  • intron variant
NC_000079.7:g.19863455G>Avariant
SNP
  • intron variant
NC_000079.7:g.19863778A>Gvariant
SNP
  • intron variant
Showing 1 - 10 of 1,650 rows
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Transgenic Alleles

No data available

Models

Model name
Experimental condition
Associated Human Diseases
Associated Phenotypes
Modifier
Source
Nme8tm1.1Arte/Nme8tm1.1Arte Txndc2tm1.1Arte/Txndc2tm1.1Arte [background:] involves: C57BL/6 * C57BL/6NTac
  • abnormal DNA repair
  • abnormal sperm physiology
MGI
Nme8tm1.1Arte/Nme8tm1.1Arte [background:] involves: C57BL/6NTacMGI
Showing 1 - 2 of 2 rows
per page

Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
Data currently unavailable; sequence viewer under construction

Sequence Details

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Expression

Primary Sources
None
Other Sources
all annotationsall anatomical structuresalimentary part of gastrointestinal systemchemosensory systemcirculatory systemendocrine systemexocrine systemhemolymphoid systemhepatobiliary systemintegumental systemmechanosensory systemmusculoskeletal systemnervous systemrenal systemreproductive systemrespiratory systemsensory systemvestibulo-auditory systemvisual systemendodermectodermmesodermmesenchymeadipose tissueappendageentire extraembryonic componentimaginal precursorpharyngeal archotherall stagesembryo stagepost embryonic, pre-adultpost-juvenile adult stageall cellular componentsextracellular regionplasma membranesynapsecell junctioncell projectioncytoplasmic vesicleendosomevacuolegolgi apparatusendoplasmic reticulumcytosolmitochondrionnucleuschromosomecytoskeletonprotein-containing complexother locations
Nme8 (Mmu)
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

No data available

Genetic Interactions

No data available