SNX3 sorting nexin 3 [Bos taurus (cattle)] - Gene

Summary

Official Symbol: SNX3provided by VGNC
Official Full Name: sorting nexin 3provided by VGNC
Primary source: VGNC:VGNC:35107
See related: BGD:BT25454; Ensembl:ENSBTAG00000018801
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: 9

Exon count:: 5

Annotation release	Status	Assembly	Chr	Location
RS_2023_09	current	ARS-UCD2.0 (GCF_002263795.3)	9	NC_037336.1 (41870929..41918141)

Chromosome 9 - NC_037336.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:: NC_037336.1 Chromosome 9 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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Markers

CC552571 (e-PCR)
- UniSTS:475734

stSG634203 (e-PCR)
- UniSTS:459882

REN49953 (e-PCR)
- UniSTS:374753

REN49968 (e-PCR)
- UniSTS:374768

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables phosphatidylinositol-3-phosphate binding	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in endocytic recycling	IEA Inferred from Electronic Annotation more info	PubMed
involved_in late endosome to Golgi transport	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in early endosome membrane	IEA Inferred from Electronic Annotation more info	PubMed
part_of retromer complex	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: sorting nexin-3

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.