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FAM189A1 (Family With Sequence Similarity 189 Member A1) is a Protein Coding gene. Diseases associated with FAM189A1 include Lung Disease, Immunodeficiency, And Chromosome Breakage Syndrome. An important paralog of this gene is FAM189B.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0016021 | integral component of membrane | IEA | -- |
This gene was present in the common ancestor of chordates.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
chimpanzee (Pan troglodytes) |
Mammalia | FAM189A1 33 32 |
|
OneToOne | |
dog (Canis familiaris) |
Mammalia | FAM189A1 33 32 |
|
OneToOne | |
rat (Rattus norvegicus) |
Mammalia | Fam189a1 32 |
|
||
mouse (Mus musculus) |
Mammalia | Fam189a1 17 33 32 |
|
||
cow (Bos Taurus) |
Mammalia | FAM189A1 33 32 |
|
OneToOne | |
oppossum (Monodelphis domestica) |
Mammalia | FAM189A1 33 |
|
OneToOne | |
platypus (Ornithorhynchus anatinus) |
Mammalia | FAM189A1 33 |
|
OneToOne | |
chicken (Gallus gallus) |
Aves | FAM189A1 33 32 |
|
OneToOne | |
lizard (Anolis carolinensis) |
Reptilia | FAM189A1 33 |
|
OneToOne | |
tropical clawed frog (Silurana tropicalis) |
Amphibia | fam189a1 32 |
|
||
zebrafish (Danio rerio) |
Actinopterygii | fam189a1 33 32 |
|
OneToOne |
SNP ID | Clin | Chr 15 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
rs199905054 | pathogenic, Lung damage, immunodeficiency and chromosome breakage syndrome, Lung disease, immunodeficiency, and chromosome breakage syndrome | 29,268,916(-) | G/A | intron_variant | |
rs886037827 | pathogenic, Lung damage, immunodeficiency and chromosome breakage syndrome, Lung disease, immunodeficiency, and chromosome breakage syndrome | 29,269,080(-) | G/A | intron_variant | |
rs1000002397 | -- | 29,281,116(-) | A/G | intron_variant | |
rs1000013013 | -- | 29,182,840(-) | AAAAAAAAA/AAAAAAAA/AAAAAAAAAA | intron_variant | |
rs1000013917 | -- | 29,204,842(-) | C/T | intron_variant |
Disorder | Aliases | PubMed IDs |
---|---|---|
lung disease, immunodeficiency, and chromosome breakage syndrome |
|
|