Homo sapiens (human): 89941
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Entry
89941 CDS
T01001
Symbol
RHOT2, ARHT2, C16orf39, MIRO-2, MIRO2, RASL
Name
(RefSeq) ras homolog family member T2
KO
K07871
mitochondrial Rho GTPase 2 [EC:3.6.5.-]
Organism
hsa
Homo sapiens (human)
Pathway
hsa04137
Mitophagy - animal
Network
nt06536
Mitophagy
Element
N01756
PINK-Parkin-independent ubiquitin-mediated mitophagy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04137 Mitophagy - animal
89941 (RHOT2)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04031 GTP-binding proteins [BR:
hsa04031
]
89941 (RHOT2)
GTP-binding proteins [BR:
hsa04031
]
Small (monomeric) G-proteins
Rho Family
Miro
89941 (RHOT2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EF_assoc_2
EF_assoc_1
Ras
Roc
EF-hand_7
Arf
AAA_16
EF-hand_6
MMR_HSR1
EF-hand_1
SRPRB
EF-hand_5
Motif
Other DBs
NCBI-GeneID:
89941
NCBI-ProteinID:
NP_620124
OMIM:
613889
HGNC:
21169
Ensembl:
ENSG00000140983
UniProt:
Q8IXI1
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:668083..674174
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AA seq
618 aa
AA seq
DB search
MRRDVRILLLGEAQVGKTSLILSLVGEEFPEEVPPRAEEITIPADVTPEKVPTHIVDYSE
AEQTDEELREEIHKANVVCVVYDVSEEATIEKIRTKWIPLVNGGTTQGPRVPIILVGNKS
DLRSGSSMEAVLPIMSQFPEIETCVECSAKNLRNISELFYYAQKAVLHPTAPLYDPEAKQ
LRPACAQALTRIFRLSDQDLDQALSDEELNAFQKSCFGHPLAPQALEDVKTVVCRNVAGG
VREDRLTLDGFLFLNTLFIQRGRHETTWTILRRFGYSDALELTADYLSPLIHVPPGCSTE
LNHLGYQFVQRVFEKHDQDRDGALSPVELQSLFSVFPAAPWGPELPRTVRTEAGRLPLHG
YLCQWTLVTYLDVRSCLGHLGYLGYPTLCEQDQAHAITVTREKRLDQEKGQTQRSVLLCK
VVGARGVGKSAFLQAFLGRGLGHQDTREQPPGYAIDTVQVNGQEKYLILCEVGTDGLLAT
SLDATCDVACLMFDGSDPKSFAHCASVYKHHYMDGQTPCLFVSSKADLPEGVAVSGPSPA
EFCRKHRLPAPVPFSCAGPAEPSTTIFTQLATMAAFPHLVHAELHPSSFWLRGLLGVVGA
AVAAVLSFSLYRVLVKSQ
NT seq
1857 nt
NT seq
+upstream
nt +downstream
nt
atgaggcgggacgtgcgcatcctgttactgggcgaggcccaggtggggaagacgtcgctg
atcctgtccctggtgggcgaggagttccccgaggaggtccctccccgcgcggaggagatc
accatccccgcggacgtcaccccggagaaggtgcccacccacatcgtggactactcagaa
gccgagcagacggacgaggagctgcgggaggagatccacaaggcaaacgtggtgtgtgtg
gtgtatgacgtctctgaggaggccaccattgagaagattcgaactaagtggatcccactg
gtgaatggggggaccacgcaggggcccagggtgcccatcatcctagtgggcaacaagtca
gacctgcggtcggggagctccatggaggccgtgctccccatcatgagccagtttcccgag
attgagacctgcgtggagtgttcggccaagaacctgaggaacatctcagagctgttctac
tacgcccagaaggccgtcctgcatcccacagcccccctctatgaccctgaggccaagcag
ttgaggcccgcgtgcgcccaggcgctgacgcgcatcttcaggctctcagatcaggacctg
gaccaggcgctcagtgacgaagagctcaacgctttccagaaatcctgctttgggcacccc
ctggccccgcaggccctggaggacgtgaagacggtggtgtgcaggaacgtggcgggcggc
gtgcgggaggaccggctgaccctggatggtttcctcttcctgaacacgctcttcatccag
cgcggccggcacgagaccacctggaccatcctgcggcgcttcggctacagcgatgccctg
gagctgactgcggactatctctcccctctgatccacgtgccccccggctgcagcacggag
ctcaaccaccttggctaccagtttgtgcagagagtgtttgagaagcacgaccaggaccgc
gacggcgccctctcgcccgtggagctgcaaagccttttcagtgtgttcccagcagcgccc
tggggccccgagctcccacgcacagtccgcacagaggccggccggttgcccctgcacgga
tacctctgccagtggaccctggtgacctacctggacgtccggagctgccttggacaccta
ggctacctgggctaccccaccctctgtgagcaggaccaggcccatgccatcacagtcact
cgtgagaagaggctggaccaggagaagggacagacgcagcggagcgtcctcctgtgcaag
gtggtaggggcccgtggagtgggcaagtctgccttcctgcaggcctttctcggccgcggc
ctggggcaccaggacacgagggagcagcctcccggctacgccatcgacacggtgcaggtc
aatggacaggagaagtacttgatcctctgtgaggtgggcacagatggtctgctggccaca
tcgctggacgccacctgtgacgttgcctgcttgatgtttgatggcagtgacccaaagtcc
tttgcacattgtgccagcgtctacaagcaccattacatggacgggcagaccccctgcctc
tttgtctcctccaaggccgacctgcccgaaggtgtcgcggtgtctggcccatcaccggcc
gagttttgccgcaagcaccggctacccgctcccgtgccgttctcctgtgctggcccagcc
gagcccagcaccaccatcttcacccagctcgccaccatggccgccttcccacatttggtc
cacgcagagctgcatccctcttccttctggctccgggggctgctgggggttgtcggggcc
gccgtggccgcagtcctcagcttctcactctacagggtcctggtgaagagccagtga
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