Free for academic non-profit institutions. Other users need a Commercial license
This gene encodes a potential transmembrane protein. [provided by RefSeq, Dec 2012]
TMEM186 (Transmembrane Protein 186) is a Protein Coding gene. Diseases associated with TMEM186 include Congenital Disorder Of Glycosylation, Type In.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005739 | mitochondrion | IDA | -- |
GO:0016020 | membrane | IEA | -- |
GO:0016021 | integral component of membrane | IEA | -- |
This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | TMEM186 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | TMEM186 30 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | Tmem186 30 |
|
||
Mouse (Mus musculus) |
Mammalia | Tmem186 30 17 31 |
|
OneToOne | |
Oppossum (Monodelphis domestica) |
Mammalia | TMEM186 31 |
|
OneToOne | |
Chicken (Gallus gallus) |
Aves | TMEM186 30 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | TMEM186 31 |
|
OneToOne | |
Tropical Clawed Frog (Silurana tropicalis) |
Amphibia | tmem186 30 |
|
||
Zebrafish (Danio rerio) |
Actinopterygii | zgc:194539 30 |
|
||
TMEM186 31 |
|
OneToOne | |||
Fruit Fly (Drosophila melanogaster) |
Insecta | CG4627 31 |
|
OneToOne |
SNP ID | Clinical significance and condition | Chr 16 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
702357 | Benign: not provided | 8,797,614(-) | T/C | INITIATIOR_CODON_VARIANT,MISSENSE_VARIANT |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv341n27 | CNV | gain | 19166990 |
dgv4906n54 | CNV | gain | 21841781 |
esv2763129 | CNV | gain | 21179565 |
esv3637841 | CNV | gain | 21293372 |
esv3637845 | CNV | gain | 21293372 |
esv3892787 | CNV | gain | 25118596 |
nsv1036281 | CNV | gain | 25217958 |
nsv1047172 | CNV | gain | 25217958 |
nsv457394 | CNV | gain | 19166990 |
nsv457398 | CNV | gain | 19166990 |
nsv476924 | CNV | novel sequence insertion | 20440878 |
nsv571424 | CNV | gain | 21841781 |
nsv571427 | CNV | gain | 21841781 |
nsv571428 | CNV | gain | 21841781 |
nsv819097 | CNV | loss | 19587683 |
Disorder | Aliases | PubMed IDs |
---|---|---|
congenital disorder of glycosylation, type in |
|
|