Gene id |
4151 |
Gene Summary Protein Summary Gene ontology Diseases PubMed |
Gene Summary
|
Gene Symbol |
MB Gene UCSC Ensembl |
Aliases |
PVALB |
Gene name |
myoglobin |
Alternate names |
myoglobin, |
Gene location |
22q12.3 (35623353: 35606763) Exons: 6 NC_000022.11
|
Gene summary(Entrez) |
This gene encodes a member of the globin superfamily and is predominantly expressed in skeletal and cardiac muscles. The encoded protein forms a monomeric globular haemoprotein that is primarily responsible for the storage and facilitated transfer of oxyg
|
OMIM |
605897 |
Protein Summary
|
Protein general information
| P02144
Name: Myoglobin
Length: 154 Mass: 17184
|
Sequence |
MGLSDGEWQLVLNVWGKVEADIPGHGQEVLIRLFKGHPETLEKFDKFKHLKSEDEMKASEDLKKHGATVLTALGG ILKKKGHHEAEIKPLAQSHATKHKIPVKYLEFISECIIQVLQSKHPGDFGADAQGAMNKALELFRKDMASNYKEL GFQG
|
Structural information |
|
Other Databases |
GeneCards: MB  Malacards: MB |
|
GO accession | Term name | Evidence code | Go category |
---|
GO:0015671 |
oxygen transport
|
IBA |
biological process |
GO:0019825 |
oxygen binding
|
IBA |
molecular function |
GO:0020037 |
heme binding
|
IEA |
molecular function |
GO:0015671 |
oxygen transport
|
IEA |
biological process |
GO:0019825 |
oxygen binding
|
IEA |
molecular function |
GO:0005344 |
oxygen carrier activity
|
IEA |
molecular function |
GO:0046872 |
metal ion binding
|
IEA |
molecular function |
GO:0015671 |
oxygen transport
|
IEA |
biological process |
GO:0015671 |
oxygen transport
|
TAS |
biological process |
GO:0005829 |
cytosol
|
TAS |
cellular component |
GO:0005829 |
cytosol
|
TAS |
cellular component |
GO:0050873 |
brown fat cell differenti ation
|
IEA |
biological process |
GO:0001666 |
response to hypoxia
|
IEA |
biological process |
GO:0043353 |
enucleate erythrocyte dif ferentiation
|
IEA |
biological process |
GO:0007507 |
heart development
|
IEA |
biological process |
GO:0042542 |
response to hydrogen pero xide
|
IEA |
biological process |
GO:0031444 |
slow-twitch skeletal musc le fiber contraction
|
IEA |
biological process |
GO:0019825 |
oxygen binding
|
IEA |
molecular function |
GO:0015671 |
oxygen transport
|
IEA |
biological process |
GO:0009725 |
response to hormone
|
IEA |
biological process |
GO:0070062 |
extracellular exosome
|
HDA |
cellular component |
GO:0015671 |
oxygen transport
|
IBA |
biological process |
GO:0019825 |
oxygen binding
|
IBA |
molecular function |
GO:0020037 |
heme binding
|
IEA |
molecular function |
GO:0015671 |
oxygen transport
|
IEA |
biological process |
GO:0019825 |
oxygen binding
|
IEA |
molecular function |
GO:0005344 |
oxygen carrier activity
|
IEA |
molecular function |
GO:0046872 |
metal ion binding
|
IEA |
molecular function |
GO:0015671 |
oxygen transport
|
IEA |
biological process |
GO:0015671 |
oxygen transport
|
TAS |
biological process |
GO:0005829 |
cytosol
|
TAS |
cellular component |
GO:0005829 |
cytosol
|
TAS |
cellular component |
GO:0050873 |
brown fat cell differenti ation
|
IEA |
biological process |
GO:0001666 |
response to hypoxia
|
IEA |
biological process |
GO:0043353 |
enucleate erythrocyte dif ferentiation
|
IEA |
biological process |
GO:0007507 |
heart development
|
IEA |
biological process |
GO:0042542 |
response to hydrogen pero xide
|
IEA |
biological process |
GO:0031444 |
slow-twitch skeletal musc le fiber contraction
|
IEA |
biological process |
GO:0019825 |
oxygen binding
|
IEA |
molecular function |
GO:0015671 |
oxygen transport
|
IEA |
biological process |
GO:0009725 |
response to hormone
|
IEA |
biological process |
GO:0070062 |
extracellular exosome
|
HDA |
cellular component |
|
|
Associated diseases |
References |
Aberrant CpGs in Low Motility Sperm | MIK: 21674046 |
Cryptorchidism | MIK: 28606200 |
|
|
PMID |
Condition |
Mutation |
Ethnicity |
Population details |
Infertility_type |
Associated_genes |
Abstract |
21674046 |
Aberrant C pGs in Low Motility Sperm
|
|
|
18
|
Male infertility |
GSE26881
|
Show abstract |
28606200 |
Cryptorchi dism
|
|
|
Monozgotic twin s (1 control, I cwith cryptorc hidism)
|
Male infertility |
MeDIP-Seq
|
Show abstract |
|