FGFR1OP2 FGFR1 oncogene partner 2 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: FGFR1OP2provided by VGNC
Official Full Name: FGFR1 oncogene partner 2provided by VGNC
Primary source: VGNC:VGNC:72551
See related: Ensembl:ENSMMUG00000006468
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
NEW: Try the new Gene table
Try the new Transcript table

Genomic context

Location:: chromosome: 11

Exon count:: 7

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	11	NC_041764.1 (28260118..28288589)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	11	NC_027903.1 (27946904..27975397)

Chromosome 11 - NC_041764.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to reference sequence details

Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

Go to the top of the page Help

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

General gene information

Go to the top of the page Help

Markers

RH93010 (e-PCR)
- UniSTS:92352

RH80150 (e-PCR)
- UniSTS:92398

SHGC-57928 (e-PCR)
- UniSTS:30712

Gene Ontology Provided by RefSeq

Process	Evidence Code	Pubs
involved_in response to wounding	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

Go to the top of the page Help

Preferred Names: FGFR1 oncogene partner 2

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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.