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)
Pathway
hsa03010
Ribosome
Disease
H00891
Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09122 Translation
03010 Ribosome
51649 (MRPS23)
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
PDBj
LinkDB
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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