Homo sapiens (human): 65993
Help
Entry
65993 CDS
T01001
Symbol
MRPS34, COXPD32, MRP-S12, MRP-S34, MRPS12, mS34
Name
(RefSeq) mitochondrial ribosomal protein S34
KO
K17412
small subunit ribosomal protein S34
Organism
hsa
Homo sapiens (human)
Pathway
hsa03010
Ribosome
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09122 Translation
03010 Ribosome
65993 (MRPS34)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03011 Ribosome [BR:
hsa03011
]
65993 (MRPS34)
Ribosome [BR:
hsa03011
]
Ribosomal proteins
Mitochondria/ Chloroplast
Small subunit
65993 (MRPS34)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MRP-S34
Motif
Other DBs
NCBI-GeneID:
65993
NCBI-ProteinID:
NP_076425
OMIM:
611994
HGNC:
16618
Ensembl:
ENSG00000074071
UniProt:
P82930
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:complement(1771895..1773134)
Genome browser
AA seq
218 aa
AA seq
DB search
MARKKVRPRLIAELARRVRALREQLNRPRDSQLYAVDYETLTRPFSGRRLPVRAWADVRR
ESRLLQLLGRLPLFGLGRLVTRKSWLWQHDEPCYWRLTRVRPDYTAQNLDHGKAWGILTF
KGKTESEAREIEHVMYHDWRLVPKHEEEAFTAFTPAPEDSLASVPYPPLLRAMIIAERQK
NGDTSTEEPMLNVQRIRMEPWDYPAKQEDKGRAKGTPV
NT seq
657 nt
NT seq
+upstream
nt +downstream
nt
atggcgcggaagaaggtgcgtccgcggctgatcgcggagctggcccgccgcgtgcgcgcc
ctgcgggagcaactgaacaggccgcgcgactcccagctctacgcggtggactacgagacc
ttgacgcggccgttctctggacgccggctgccggtccgggcctgggccgacgtgcgccgc
gagagccgcctcttgcagctgctcggccgcctcccgctcttcggcctgggccgcctggtc
acgcgcaagtcctggctgtggcagcacgacgagccgtgctactggcgcctcacgcgggtg
cggcccgactacacggcgcagaacttggaccacgggaaggcctggggcatcctgaccttc
aaagggaagactgagagcgaggcgcgggagatcgaacacgtcatgtaccatgactggcgg
ctggtgcccaagcacgaggaggaggccttcaccgcgttcacgccggcgccggaagacagc
ctggcctccgtgccgtacccgcctctcctccgggccatgattatcgcagaacgacagaaa
aatggagacacaagcaccgaggagcccatgctgaatgtgcagaggatacgcatggaaccc
tgggattaccctgcaaaacaggaagacaaaggaagggccaagggcacccccgtctag
DBGET
integrated database retrieval system
