Gene id |
26515 |
Gene Summary Protein Summary Gene ontology Diseases PubMed |
Gene Summary
|
Gene Symbol |
TIMM10B Gene UCSC Ensembl |
Aliases |
FXC1, TIM10B, Tim9b |
Gene name |
translocase of inner mitochondrial membrane 10B |
Alternate names |
mitochondrial import inner membrane translocase subunit Tim10 B, fracture callus 1 homolog, fracture callus protein 1, mitochondrial import inner membrane translocase subunit Tim9 B, translocase of inner mitochondrial membrane 10 homolog B, |
Gene location |
11p15.4 (6481500: 6484680) Exons: 3 NC_000011.10
|
Gene summary(Entrez) |
FXC1, or TIMM10B, belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the
|
OMIM |
0 |
Protein Summary
|
Protein general information
| Q9Y5J6
Name: Mitochondrial import inner membrane translocase subunit Tim10 B (Fracture callus protein 1) (FxC1) (Mitochondrial import inner membrane translocase subunit Tim9 B) (TIMM10B) (Tim10b)
Length: 103 Mass: 11586
Tissue specificity: Ubiquitous, with highest expression in heart, kidney, liver and skeletal muscle. {ECO
|
Sequence |
MERQQQQQQQLRNLRDFLLVYNRMTELCFQRCVPSLHHRALDAEEEACLHSCAGKLIHSNHRLMAAYVQLMPALV QRRIADYEAASAVPGVAAEQPGVSPSGS
|
Structural information |
|
Other Databases |
GeneCards: TIMM10B  Malacards: TIMM10B |
|
GO accession | Term name | Evidence code | Go category |
---|
GO:0042719 |
mitochondrial intermembra ne space protein transpor ter complex
|
IBA |
cellular component |
GO:0042721 |
TIM22 mitochondrial impor t inner membrane insertio n complex
|
IDA |
cellular component |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0046872 |
metal ion binding
|
IEA |
molecular function |
GO:0015031 |
protein transport
|
IEA |
biological process |
GO:0005743 |
mitochondrial inner membr ane
|
IEA |
cellular component |
GO:0016020 |
membrane
|
IEA |
cellular component |
GO:0015031 |
protein transport
|
IEA |
biological process |
GO:0005739 |
mitochondrion
|
IEA |
cellular component |
GO:0007160 |
cell-matrix adhesion
|
TAS |
biological process |
GO:0005743 |
mitochondrial inner membr ane
|
TAS |
cellular component |
GO:0006626 |
protein targeting to mito chondrion
|
TAS |
biological process |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0042719 |
mitochondrial intermembra ne space protein transpor ter complex
|
IDA |
cellular component |
GO:0005743 |
mitochondrial inner membr ane
|
IDA |
cellular component |
GO:0005758 |
mitochondrial intermembra ne space
|
TAS |
cellular component |
GO:0005743 |
mitochondrial inner membr ane
|
IEA |
cellular component |
|
|
Associated diseases |
References |
Aberrant CpGs in Low Motility Sperm | MIK: 21674046 |
Teratozoospermia | MIK: 17327269 |
|
|
PMID |
Condition |
Mutation |
Ethnicity |
Population details |
Infertility_type |
Associated_genes |
Abstract |
17327269 |
Teratozoos permia
|
|
|
19 (6 controls , 13 cases)
|
Male infertility |
GSE6872 analyzed by GEO2R (cutoff 1.5 fold)
|
Show abstract |
21674046 |
Aberrant C pGs in Low Motility Sperm
|
|
|
18
|
Male infertility |
GSE26881
|
Show abstract |
|