CNOT9 CCR4-NOT transcription complex subunit 9 [Equus caballus (horse)] - Gene

Summary

Official Symbol: CNOT9provided by VGNC
Official Full Name: CCR4-NOT transcription complex subunit 9provided by VGNC
Primary source: VGNC:VGNC:16682
See related: Ensembl:ENSECAG00000059139
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Equus caballus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Perissodactyla; Equidae; Equus
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 6

Exon count:: 9

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	EquCab3.0 (GCF_002863925.1)	6	NC_009149.3 (7962229..7991868)

Chromosome 6 - NC_009149.3 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:: NC_009149.3 Chromosome 6 Reference EquCab3.0 Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

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 RefSeq

Process	Evidence Code	Pubs
involved_in mRNA catabolic process	IEA Inferred from Electronic Annotation more info	PubMed
involved_in negative regulation of translation	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
part_of CCR4-NOT complex	IEA Inferred from Electronic Annotation more info	PubMed
part_of CCR4-NOT core complex	IEA Inferred from Electronic Annotation more info	PubMed
located_in P-body	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: CCR4-NOT transcription complex subunit 9

Names: cell differentiation protein RCD1 homolog

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.