Cimap1c ciliary microtubule associated protein 1C [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: Cimap1cprovided by RGD
Official Full Name: ciliary microtubule associated protein 1Cprovided by RGD
Primary source: RGD:1304976
See related: EnsemblRapid:ENSRNOG00000027109 AllianceGenome:RGD:1304976
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Rattus norvegicus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Also known as: Odf3l1; RGD1304976
Summary: Predicted to be active in cytoskeleton. Orthologous to human CIMAP1C (ciliary microtubule associated protein 1C). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Biased expression in Testes (RPKM 31.2), Uterus (RPKM 12.1) and 6 other tissues See more
Orthologs: human mouse all
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Genomic context

Location:: 8q24

Exon count:: 9

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	8	NC_086026.1 (66144726..66176985, complement)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	8	NC_051343.1 (57248746..57281084, complement)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	8	NC_005107.4 (61516249..61542946, complement)

Chromosome 8 - NC_086026.1 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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Gene Ontology Provided by RGD

Component	Evidence Code	Pubs
is_active_in cytoskeleton	IBA Inferred from Biological aspect of Ancestor more info

General protein information

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Preferred Names: protein CIMAP1C

Names: outer dense fiber of sperm tails 3-like 1; outer dense fiber protein 3-like protein 1

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.