Gene

Cep128

Species
Rattus norvegicus
Symbol
Cep128
Name
centrosomal protein 128
Synonyms
  • centrosomal protein 128kDa
  • centrosomal protein of 128 kDa
Biotype
protein coding gene
Automated Description
Predicted to be involved in protein localization. Predicted to act upstream of or within regulation of gene expression and sperm flagellum assembly. Predicted to be located in Golgi apparatus; centrosome; and nuclear membrane. Predicted to be part of centriolar subdistal appendage. Predicted to be active in centriole and spindle pole. Orthologous to human CEP128 (centrosomal protein 128).
RGD Description
Predicted to be involved in protein localization. Predicted to act upstream of or within regulation of gene expression and sperm flagellum assembly. Predicted to be located in Golgi apparatus; microtubule cytoskeleton; and nuclear membrane. Predicted to be part of centriolar subdistal appendage. Orthologous to human CEP128 (centrosomal protein 128); INTERACTS WITH 1-naphthyl isothiocyanate; bisphenol A; clofibrate.
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR46657
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensCEP1281 of 10YesYes  
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
None
Other Sources
None
No data available

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
mRatBN7.2
Viewer Help
110.00M110.05M110.10M110.15M110.20M110.25M110.30M
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_051341.1:g.109951013G>Tvariant
SNP
  • 3 prime UTR variant
NC_051341.1:g.110196340G>Avariant
SNP
  • intron variant
variant
SNP
  • intron variant
NC_051341.1:g.110148446T>Cvariant
SNP
  • intron variant
NC_051341.1:g.110161055C>Tvariant
SNP
  • intron variant
NC_051341.1:g.110164665A>Cvariant
SNP
  • intron variant
NC_051341.1:g.110189891A>Gvariant
SNP
  • intron variant
NC_051341.1:g.110191063G>Avariant
SNP
  • intron variant
NC_051341.1:g.110191386G>Avariant
SNP
  • intron variant
NC_051341.1:g.110191624C>Tvariant
SNP
  • intron variant
Showing 1 - 10 of 1,382 rows
per page

Transgenic Alleles

No data available

Models

No data available

Sequence Feature Viewer

Genome location
Assembly version
mRatBN7.2
Viewer Help
110.00M110.05M110.10M110.15M110.20M110.25M110.30MENSRNOT00000057756.5 (Cep128)ENSRNOT00000076546.2 (Cep128)ENSRNOT00000076887.3 (Cep128)ENSRNOT00000110851.1 (Cep128)XM_056985584.2 (Cep128)XM_056985586.2 (Cep128)XM_056985587.2 (Cep128)XM_056985588.2 (Cep128)XM_056985589.2 (Cep128)XM_056985590.2 (Cep128)Maximum features displayed. See full view for more.

Sequence Details

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Expression

Primary Sources
None
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