RND2 Rho family GTPase 2 [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: RND2provided by VGNC
Official Full Name: Rho family GTPase 2provided by VGNC
Primary source: VGNC:VGNC:76765
See related: Ensembl:ENSMMUG00000065269
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: 16

Exon count:: 5

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	16	NC_041769.1 (54166488..54171406)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	16	NC_027908.1 (48895591..48900495)

Chromosome 16 - NC_041769.1 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

NoName (e-PCR)
- UniSTS:488228

NoName (e-PCR)
- UniSTS:490549

MARC_7249-7250:996687691:1 (e-PCR)
- UniSTS:269749

RH98686 (e-PCR)
- UniSTS:92889

RH69062 (e-PCR)
- UniSTS:26610

Gene Ontology Provided by RefSeq

Function	Evidence Code	Pubs
enables GTP binding	IEA Inferred from Electronic Annotation more info	PubMed
enables GTPase activity	IEA Inferred from Electronic Annotation more info	PubMed

Process	Evidence Code	Pubs
involved_in small GTPase-mediated signal transduction	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: rho-related GTP-binding protein RhoN

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.