Homo sapiens (human): 4151
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Entry
4151 CDS
T01001
Symbol
MB, MYOSB, PVALB
Name
(RefSeq) myoglobin
KO
K21892
myoglobin
Organism
hsa
Homo sapiens (human)
Disease
H02805
Sarcoplasmic body myopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
4151 (MB)
Transporters [BR:
hsa02000
]
Other transporters
Pores ion channels [TC:
1
]
4151 (MB)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Globin
LpxI_N
Motif
Other DBs
NCBI-GeneID:
4151
NCBI-ProteinID:
NP_005359
OMIM:
160000
HGNC:
6915
Ensembl:
ENSG00000198125
UniProt:
P02144
A0A1K0FU49
Structure
PDB
PDBj
LinkDB
All DBs
Position
22:complement(35606764..35623354)
Genome browser
AA seq
154 aa
AA seq
DB search
MGLSDGEWQLVLNVWGKVEADIPGHGQEVLIRLFKGHPETLEKFDKFKHLKSEDEMKASE
DLKKHGATVLTALGGILKKKGHHEAEIKPLAQSHATKHKIPVKYLEFISECIIQVLQSKH
PGDFGADAQGAMNKALELFRKDMASNYKELGFQG
NT seq
465 nt
NT seq
+upstream
nt +downstream
nt
atggggctcagcgacggggaatggcagttggtgctgaacgtctgggggaaggtggaggct
gacatcccaggccatgggcaggaagtcctcatcaggctctttaagggtcacccagagact
ctggagaagtttgacaagttcaagcacctgaagtcagaggacgagatgaaggcgtctgag
gacttaaagaagcatggtgccaccgtgctcaccgccctgggtggcatccttaagaagaag
gggcatcatgaggcagagattaagcccctggcacagtcgcatgccaccaagcacaagatc
cccgtgaagtacctggagttcatctcggaatgcatcatccaggttctgcagagcaagcat
cccggggactttggtgctgatgcccagggggccatgaacaaggccctggagctgttccgg
aaggacatggcctccaactacaaggagctgggcttccagggctag
DBGET
integrated database retrieval system
