Homo sapiens (human): 51021
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Entry
51021 CDS
T01001
Symbol
MRPS16, CGI-132, COXPD2, MRP-S16, RPMS16, S16mt, bS16m
Name
(RefSeq) mitochondrial ribosomal protein S16
KO
K02959
small subunit ribosomal protein S16
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
51021 (MRPS16)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03011 Ribosome [BR:
hsa03011
]
51021 (MRPS16)
Ribosome [BR:
hsa03011
]
Ribosomal proteins
Mitochondria/ Chloroplast
Small subunit
51021 (MRPS16)
Bacteria
51021 (MRPS16)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ribosomal_S16
FtsK_4TM
Motif
Other DBs
NCBI-GeneID:
51021
NCBI-ProteinID:
NP_057149
OMIM:
609204
HGNC:
14048
Ensembl:
ENSG00000182180
UniProt:
Q9Y3D3
Structure
PDB
PDBj
LinkDB
All DBs
Position
10:complement(73248849..73252644)
Genome browser
AA seq
137 aa
AA seq
DB search
MVHLTTLLCKAYRGGHLTIRLALGGCTNRPFYRIVAAHNKCPRDGRFVEQLGSYDPLPNS
HGEKLVALNLDRIRHWIGCGAHLSKPMEKLLGLAGFFPLHPMMITNAERLRRKRAREVLL
ASQKTDAEATDTEATET
NT seq
414 nt
NT seq
+upstream
nt +downstream
nt
atggtccacctcactactctcctctgcaaggcctaccgtgggggccacttaaccatccgc
cttgccctgggtggctgcaccaatcggccgttctaccgcattgtggctgctcacaacaag
tgtcccagggatggccgtttcgtagagcagctgggctcctatgatccattgcccaacagt
catggagaaaaactcgttgccctcaacctagacaggatccgtcattggattggctgcggg
gcccacctctctaagcctatggaaaagcttctgggtcttgctggctttttccctctgcat
cctatgatgatcacaaatgctgagagactgcgaaggaaacgggcacgtgaagtcctgtta
gcttctcagaaaacagatgcagaagctacagatacagaggctacagaaacataa
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integrated database retrieval system
