Homo sapiens (human): 28957
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Entry
28957 CDS
T01001
Symbol
MRPS28, COXPD47, HSPC007, MRP-S28, MRP-S35, MRPS35
Name
(RefSeq) mitochondrial ribosomal protein S28
KO
K17407
small subunit ribosomal protein S28
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
]
28957 (MRPS28)
Ribosome [BR:
hsa03011
]
Ribosomal proteins
Mitochondria/ Chloroplast
Small subunit
28957 (MRPS28)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MRP-S35
S1
Motif
Other DBs
NCBI-GeneID:
28957
NCBI-ProteinID:
NP_054737
OMIM:
611990
HGNC:
14513
Ensembl:
ENSG00000147586
UniProt:
Q9Y2Q9
A0A0S2Z563
Structure
PDB
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All DBs
Position
8:complement(79918717..80030259)
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AA seq
187 aa
AA seq
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MAALCRTRAVAAESHFLRVFLFFRPFRGVGTESGSESGSSNAKEPKTRAGGFASALERHS
ELLQKVEPLQKGSPKNVESFASMLRHSPLTQMGPAKDKLVIGRIFHIVENDLYIDFGGKF
HCVCRRPEVDGEKYQKGTRVRLRLLDLELTSRFLGATTDTTVLEANAVLLGIQESKDSRS
KEEHHEK
NT seq
564 nt
NT seq
+upstream
nt +downstream
nt
atggcggcgctgtgtcggacccgtgctgtggctgccgagagccattttctgcgagtgttt
ctcttcttcaggccctttcggggtgtaggcactgagagtggatccgaaagtggtagttcc
aatgccaaggagcctaagacgcgcgcaggcggtttcgcgagcgcgttggagcggcactcg
gagcttctacagaaggtggagcccctacagaagggttctccaaaaaatgtggaatccttt
gcatctatgctgagacattctcctcttacacagatgggacctgcaaaggataaactggtc
attggacggatctttcatattgtggagaatgatctgtacatagattttggtggaaagttt
cattgtgtatgtagaagaccagaagtggatggagagaaataccagaaaggaaccagggtc
cggttgcggctattagatcttgaacttacgtctaggttcctgggagcaacaacagataca
actgtactagaggctaatgcagttctcttgggaatccaggagagtaaagactcaagatcg
aaagaagaacatcatgaaaaataa
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