Homo sapiens (human): 51649
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Entry
51649 CDS
T01001
Symbol
MRPS23, CGI-138, COXPD46, HSPC329, MRP-S23, mS23
Name
(RefSeq) mitochondrial ribosomal protein S23
KO
K17402
small subunit ribosomal protein S23
Organism
hsa
Homo sapiens (human)
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03011 Ribosome [BR:
hsa03011
]
51649 (MRPS23)
Ribosome [BR:
hsa03011
]
Ribosomal proteins
Mitochondria/ Chloroplast
Small subunit
51649 (MRPS23)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MRP-S23
MRP-S25
Motif
Other DBs
NCBI-GeneID:
51649
NCBI-ProteinID:
NP_057154
OMIM:
611985
HGNC:
14509
Ensembl:
ENSG00000181610
UniProt:
Q9Y3D9
Structure
PDB
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All DBs
Position
17:complement(57834781..57850044)
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AA seq
190 aa
AA seq
DB search
MAGSRLETVGSIFSRTRDLVRAGVLKEKPLWFDVYDAFPPLREPVFQRPRVRYGKAKAPI
QDIWYHEDRIRAKFYSVYGSGQRAFDLFNPNFKSTCQRFVEKYTELQKLGETDEEKLFVE
TGKALLAEGVILRRVGEARTQHGGSHVSRKSEHLSVRPQTALEENETQKEVPQDQHLEAP
ADQSKGLLPP
NT seq
573 nt
NT seq
+upstream
nt +downstream
nt
atggcaggcagccggctggaaaccgtagggagcatcttctctcggactcgggacctggtt
cgggccggggtgctgaaggagaagcccctgtggtttgacgtatatgacgcctttcccccg
ctgagggagcccgtcttccaaaggcctcgagtgcgatatggcaaagccaaagctcccatc
caagacatctggtaccacgaggatcggattagagcgaagttttattcagtgtatgggtct
ggtcaaagagcttttgatctattcaatccaaacttcaagtctacctgtcaacggtttgtg
gagaagtacactgagctacagaaacttggagaaacagatgaagagaagttatttgtggaa
acagggaaggctttattggcagaaggtgtcattttaagacgagtaggcgaagcaaggact
caacacggaggtagtcacgtttcccggaaatccgaacacttgagtgtcagaccacagact
gcgttggaagaaaacgagactcagaaagaagttccacaggaccagcatttggaggcacct
gcagaccagtcgaaaggtctcttgcctccctga
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