Homo sapiens (human): 64432
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Entry
64432 CDS
T01001
Symbol
MRPS25, COXPD50, MRP-S25, RPMS25, mS25
Name
(RefSeq) mitochondrial ribosomal protein S25
KO
K17404
small subunit ribosomal protein S25
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
64432 (MRPS25)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03011 Ribosome [BR:
hsa03011
]
64432 (MRPS25)
Ribosome [BR:
hsa03011
]
Ribosomal proteins
Mitochondria/ Chloroplast
Small subunit
64432 (MRPS25)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
L51_S25_CI-B8
DUF6387
CobW_C_DAAF9
DUF3438
Motif
Other DBs
NCBI-GeneID:
64432
NCBI-ProteinID:
NP_071942
OMIM:
611987
HGNC:
14511
Ensembl:
ENSG00000131368
UniProt:
P82663
Structure
PDB
PDBj
LinkDB
All DBs
Position
3:complement(15042251..15065315)
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AA seq
173 aa
AA seq
DB search
MPMKGRFPIRRTLQYLSQGNVVFKDSVKVMTVNYNTHGELGEGARKFVFFNIPQIQYKNP
WVQIMMFKNMTPSPFLRFYLDSGEQVLVDVETKSNKEIMEHIRKILGKNEETLREEEEEK
KQLSHPANFGPRKYCLRECICEVEGQVPCPSLVPLPKEMRGKYKAALKADAQD
NT seq
522 nt
NT seq
+upstream
nt +downstream
nt
atgcccatgaagggccgcttccccatccgccgcaccctgcaatatctgagccaggggaac
gtggtgttcaaggactccgtgaaggtcatgacagtgaattacaacacgcatggggagctg
ggcgagggcgccaggaagtttgtgtttttcaacatacctcagattcaatacaaaaaccct
tgggtgcagatcatgatgtttaagaacatgacgccgtcacccttcctgcgattctactta
gattctggggagcaggtcctggtggatgtggagaccaagagcaataaggagatcatggag
cacatcagaaaaatcttggggaagaatgaggaaaccctcagggaagaggaggaggagaaa
aagcagctttctcacccagccaacttcggccctcgaaagtactgcctgcgggagtgcatc
tgtgaagtggaagggcaggtgccctgccccagcctggtgccattacccaaggagatgagg
gggaagtacaaagccgctctgaaagccgatgcccaggactaa
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integrated database retrieval system
