Cep295nl CEP295 N-terminal like [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: Cep295nlprovided by RGD
Official Full Name: CEP295 N-terminal likeprovided by RGD
Primary source: RGD:1597046
See related: EnsemblRapid:ENSRNOG00000033143 AllianceGenome:RGD:1597046
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Rattus norvegicus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Also known as: Ddc8
Summary: Predicted to enable microtubule binding activity. Predicted to be involved in regulation of centriole replication. Predicted to be located in motile cilium. Predicted to be active in centriole; centrosome; and cytosol. Orthologous to human CEP295NL (CEP295 N-terminal like). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Biased expression in Testes (RPKM 250.2), Lung (RPKM 52.4) and 7 other tissues See more
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Genomic context

Location:: 10q32.3

Exon count:: 2

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	10	NC_086028.1 (104066652..104079787, complement)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	10	NC_051345.1 (103562190..103581183, complement)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	10	NC_005109.4 (107363511..107381280, complement)

Chromosome 10 - NC_086028.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

Ddc8 (e-PCR), detects polymorphism
- UniSTS:532065

Gene Ontology Provided by RGD

Component	Evidence Code	Pubs
located_in motile cilium	ISO Inferred from Sequence Orthology more info

General protein information

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Preferred Names: protein DDC8 homolog

Names: differential display clone 8

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.