Gene: RHOT2 (ras homolog family member T2)  Homo sapiens

Symbol: RHOT2
Name: ras homolog family member T2
Description: This gene encodes a member of the Rho family of GTPases. The encoded protein is localized to the outer mitochondrial membrane and plays a role in mitochondrial trafficking and fusion-fission dynamics. [provided by RefSeq, Nov 2011]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ARHT2; C16orf39; hMiro-2; MIRO-2; MIRO2; mitochondrial Rho (MIRO) GTPase 2; mitochondrial Rho 2; mitochondrial Rho GTPase 2; OTTHUMP00000149943; ras homolog gene family, member T2; RASL
Orthologs: Mus musculus : Rhot2 (ras homolog gene family, member T2)  MGI
Rattus norvegicus : Rhot2 (ras homolog family member T2)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_116655,726 - 661,817+NCBI
Human Genome Assembly HuRef16639,868 - 645,999+NCBI
Human Genome Assembly GRCh3716718,083 - 724,174+NCBI
Human Celera Assembly16918,290 - 924,328+NCBI
Human Genome Assembly Build 3616658,134 - 664,172+NCBI
Human Cytogenetic Map16p13.3 NCBI
Human Genome Assembly16658,133 - 664,171 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on RHOT2
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1347429
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-03-06
Status: ACTIVE