SLU7 SLU7 homolog, splicing factor [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: SLU7provided by VGNC
Official Full Name: SLU7 homolog, splicing factorprovided by VGNC
Primary source: VGNC:VGNC:77728
See related: Ensembl:ENSMMUG00000023075
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 6

Exon count:: 16

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	6	NC_041759.1 (157789368..157805590, complement)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	6	NC_027898.1 (158600777..158616752, complement)

Chromosome 6 - NC_041759.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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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Markers

PMC316594P1 (e-PCR)
- UniSTS:273017

D5S1599E (e-PCR)
- UniSTS:151020

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables pre-mRNA 3'-splice site binding	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in mRNA splicing, via spliceosome	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
part_of spliceosomal complex	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: pre-mRNA-splicing factor SLU7

Names: SLU7 splicing factor 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.