PRPF18 pre-mRNA processing factor 18 [Bos taurus (cattle)] - Gene

Summary

Gene symbol: PRPF18
Gene description: pre-mRNA processing factor 18
See related: BGD:BT30450; Ensembl:ENSBTAG00000017244
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Bos taurus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Artiodactyla; Ruminantia; Pecora; Bovidae; Bovinae; Bos
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 13

Exon count:: 11

Annotation release	Status	Assembly	Chr	Location
RS_2023_09	current	ARS-UCD2.0 (GCF_002263795.3)	13	NC_037340.1 (28284969..28341091)

Chromosome 13 - NC_037340.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

Genomic Sequence:: NC_037340.1 Chromosome 13 Reference ARS-UCD2.0 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 RNA splicing	IEA Inferred from Electronic Annotation more info	PubMed
involved_in generation of catalytic spliceosome for second transesterification step	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
part_of U2-type post-spliceosomal complex	IEA Inferred from Electronic Annotation more info	PubMed
part_of U4/U6 x U5 tri-snRNP complex	IEA Inferred from Electronic Annotation more info	PubMed
part_of U5 snRNP	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: pre-mRNA-splicing factor 18

Names: PRP18 homolog; PRP18 pre-mRNA processing factor 18 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.