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TIMM29 (Translocase Of Inner Mitochondrial Membrane 29) is a Protein Coding gene. Diseases associated with TIMM29 include Sengers Syndrome and Visual Cortex Disease.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005515 | protein binding | IPI | 27554484 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005739 | mitochondrion | IEA | -- |
GO:0005743 | mitochondrial inner membrane | IEA,IDA | 27554484 |
GO:0005758 | mitochondrial intermembrane space | IDA | 27554484 |
GO:0016020 | membrane | IEA | -- |
GO:0016021 | integral component of membrane | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0015031 | protein transport | IEA | -- |
GO:0045039 | protein import into mitochondrial inner membrane | IDA,IMP | 27554484 |
This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | C19H19orf52 30 |
|
||
C19orf52 31 |
|
OneToOne | |||
Dog (Canis familiaris) |
Mammalia | C20H19orf52 30 |
|
||
C19orf52 31 |
|
OneToOne | |||
Cow (Bos Taurus) |
Mammalia | C7H19orf52 30 31 |
|
OneToOne | |
Mouse (Mus musculus) |
Mammalia | 1810026J23Rik 30 31 |
|
OneToOne | |
Timm29 17 |
|
||||
Rat (Rattus norvegicus) |
Mammalia | RGD1309188 30 |
|
||
Oppossum (Monodelphis domestica) |
Mammalia | C19orf52 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | C19orf52 31 |
|
OneToOne | |
Tropical Clawed Frog (Silurana tropicalis) |
Amphibia | c19orf52 30 |
|
||
Zebrafish (Danio rerio) |
Actinopterygii | zgc:110046 30 |
|
||
C3H19orf52 31 |
|
OneToOne | |||
African malaria mosquito (Anopheles gambiae) |
Insecta | AgaP_AGAP001454 30 |
|
||
Fruit Fly (Drosophila melanogaster) |
Insecta | CG14270 30 31 |
|
OneToOne | |
Worm (Caenorhabditis elegans) |
Secernentea | R04F11.5 31 |
|
OneToOne | |
Sea Squirt (Ciona savignyi) |
Ascidiacea | -- 31 |
|
OneToOne |
Disorder | Aliases | PubMed IDs |
---|---|---|
sengers syndrome |
|
|
visual cortex disease |
|
|
visual pathway disease |
|
|
mohr-tranebjaerg syndrome |
|
|
cortical blindness |
|
|