Homo sapiens (human): 91574
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Entry
91574 CDS
T01001
Symbol
MTRFR, C12orf65, COXPD7, SPG55, mtRF-R
Name
(RefSeq) mitochondrial translation release factor in rescue
KO
K23498
peptide chain release factor
Organism
hsa
Homo sapiens (human)
Disease
H00266
Hereditary spastic paraplegia
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
91574 (MTRFR)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial DNA transcription, translation, and replication factors
Mitochondrial transcription and translation factors
Other mitochondrial DNA transcription and translation factors
91574 (MTRFR)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
RF-1
Motif
Other DBs
NCBI-GeneID:
91574
NCBI-ProteinID:
NP_001137377
OMIM:
613541
HGNC:
26784
Ensembl:
ENSG00000130921
UniProt:
Q9H3J6
Structure
PDB
PDBj
LinkDB
All DBs
Position
12:123232914..123257960
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AA seq
166 aa
AA seq
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MSTVGLFHFPTPLTRICPAPWGLRLWEKLTLLSPGIAVTPVQMAGKKDYPALLSLDENEL
EEQFVKGHGPGGQATNKTSNCVVLKHIPSGIVVKCHQTRSVDQNRKLARKILQEKVDVFY
NGENSPVHKEKREAAKKKQERKKRAKETLEKKKLLKELWESSKKVH
NT seq
501 nt
NT seq
+upstream
nt +downstream
nt
atgagcaccgtgggtttatttcattttcctacaccactgacccgaatatgcccggcgcca
tggggactccggctttgggagaagctgacgttgttatccccaggaatagctgtcactccg
gtccagatggcaggcaagaaggactaccctgcactgctttccttggatgagaatgaactc
gaagagcagtttgtgaaaggacacggtccagggggccaggcaaccaacaaaaccagcaac
tgcgtggtgctgaagcacatcccctcaggcatcgttgtaaagtgccatcagacaagatca
gttgatcagaacagaaagctagctcggaaaatcctacaagagaaagtagatgttttctac
aatggtgaaaacagtcctgttcacaaagaaaaacgagaagcggcgaagaaaaaacaagaa
aggaaaaaaagagcaaaggaaaccctggaaaaaaagaagctacttaaagaactgtgggag
tcaagtaaaaaggtccactga
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