Gene

rmh-2

Species
Caenorhabditis elegans
Symbol
rmh-2
Name
RMi1 (RMI1) Homolog 2
Synonyms
  • CELE_T07C12.12
  • T07C12.12
Biotype
protein coding gene
Automated Description
Predicted to enable nucleotide binding activity. Involved in larval development. Predicted to be part of RecQ family helicase-topoisomerase III complex. Predicted to be active in nuclear body. Orthologous to human RMI1 (RecQ mediated genome instability 1).
WB Description
Predicted to enable nucleotide binding activity. Involved in larval development. Predicted to be located in nuclear body. Predicted to be part of RecQ family helicase-topoisomerase III complex. Is an ortholog of human RMI1 (RecQ mediated genome instability 1).
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR14790
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensRMI17 of 9YesYes   
Mus musculusRmi17 of 9YesYes   
Rattus norvegicusRmi16 of 9YesYes   
Xenopus tropicalisrmi16 of 9YesYes   
Danio reriormi16 of 9YesYes   
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
rmh-1156939223 of 8  

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None
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
rmh-2 (Cel)
RMI1 (Hsa)
Rmi1 (Mmu)
Rmi1 (Rno)
rmi1 (Xtr)
Cell color indicative of annotation volume
No data available

Alleles and Variants

Genome location
Assembly version
WBcel235
Viewer Help
9.9280M9.9285M9.9290M9.9295M9.9300M9.9305M
Variant Types and ConsequencesOnly variants associated to alleles are shown in the graphics above. See all variants in JBrowse.
Allele/Variant Symbol
Allele Synonyms
Category
Variant
Variant type
Molecular consequence
Has Disease Annotations
Has Phenotype Annotations
NC_003283.11:g.9929782G>Avariant
SNP
  • missense variant
NC_003283.11:g.9929785G>Avariant
SNP
  • missense variant
NC_003283.11:g.9927936G>Avariant
SNP
  • synonymous variant
NC_003283.11:g.9928223G>Avariant
SNP
  • intron variant
NC_003283.11:g.9928662C>Tvariant
SNP
  • missense variant
NC_003283.11:g.9929061A>Cvariant
SNP
  • synonymous variant
NC_003283.11:g.9929783A>Cvariant
SNP
  • missense variant
NC_003283.11:g.9929783A>Tvariant
SNP
  • missense variant
NC_003283.11:g.9929673C>Tvariant
SNP
  • synonymous variant
NC_003283.11:g.9928160G>Avariant
SNP
  • intron variant
Showing 1 - 10 of 37 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
WBcel235
Viewer Help
9.9280M9.9285M9.9290M9.9295M9.9300M9.9305MT07C12.12.1 (rmh-2)C50H2.13.1 (C50H2.13)

Sequence Details

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Expression

Primary Sources
Other Sources
Must provide at least one subject
Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

Molecular Interactions

2 interactor genes based on 4 annotations
rmh-2 molecule type
Interactor gene
Interactor species
Interactor molecule type
Detection methods
Source
Reference
protein
top-3ACaenorhabditis elegans
protein
  • two hybrid
PMID:35639927
protein
top-3ACaenorhabditis elegans
protein
  • affinity chromatography technology
PMID:35639927
protein
top-3ACaenorhabditis elegans
protein
  • affinity chromatography technology
PMID:35639927
protein
ubq-1Caenorhabditis elegans
protein
  • affinity chromatography technology
PMID:34321666
Showing 1 - 4 of 4 rows
per page

Genetic Interactions

No data available