Gene

BC048562

Species
Mus musculus
Symbol
BC048562
Name
cDNA sequence BC048562
Synonyms
None
Biotype
protein coding gene
Automated Description
Is expressed in ovary and testis. Orthologous to human CIMIP7 (ciliary microtubule inner protein 7).
MGI Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR35539
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensCIMIP710 of 10YesYes  
Rattus norvegicusCimip79 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

No paralogs for the gene.

Function - GO Annotations

No function available for that gene

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
Phenotype Term
Annotation details
References
abnormal locomotor behavior
abnormal sensory capabilities/reflexes/nociception
decreased fasting circulating glucose level
decreased locomotor activity
increased freezing behavior
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Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume

Alleles and Variants

Genome location
Assembly version
GRCm39
Viewer Help
108.314M108.315M108.316M108.317M108.318M108.319M108.320M108.321M108.322M108.323M
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
BC048562em2Cya
  • BC048562em1flox
allele
BC048562tm1b(KOMP)Wtsiallele
Yes
BC048562tm1a(KOMP)Wtsiallele
NC_000075.7:g.108317002C>Tvariant
SNP
  • intron variant
NC_000075.7:g.108314348T>Cvariant
SNP
  • intron variant
NC_000075.7:g.108314718G>Avariant
SNP
  • intron variant
NC_000075.7:g.108319879C>Avariant
SNP
  • intron variant
NC_000075.7:g.108318332A>Cvariant
SNP
  • intron variant
NC_000075.7:g.108315092G>Avariant
SNP
  • intron variant
NC_000075.7:g.108320092A>Gvariant
SNP
  • intron variant
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Transgenic Alleles

No data available

Models

Model name
Experimental condition
Associated Human Diseases
Associated Phenotypes
Modifier
Source
BC048562tm1b(KOMP)Wtsi/BC048562tm1b(KOMP)Wtsi [background:] C57BL/6N-BC048562tm1b(KOMP)Wtsi/Bay
  • abnormal locomotor behavior
  • abnormal sensory capabilities/reflexes/nociception
MGI
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Sequence Feature Viewer

Genome location
Assembly version
GRCm39
Viewer Help
108.314M108.315M108.316M108.317M108.318M108.319M108.320M108.321M108.322M108.323M

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

No data available

Genetic Interactions

No data available