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)
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
]
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
Motif
Other DBs
NCBI-GeneID:
64432
NCBI-ProteinID:
NP_071942
OMIM:
611987
HGNC:
14511
Ensembl:
ENSG00000131368
UniProt:
P82663
Structure
PDB
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All DBs
Position
3:complement(15042251..15065315)
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AA seq
173 aa
AA seq
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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