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FNDC3A (Fibronectin Type III Domain Containing 3A) is a Protein Coding gene. Diseases associated with FNDC3A include Deafness, Autosomal Dominant 56 and Deafness, Autosomal Recessive 100. An important paralog of this gene is FNDC3B.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0003723 | RNA binding | HDA | 22658674 |
GO:0005515 | protein binding | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0000139 | Golgi membrane | IEA | -- |
GO:0001669 | acrosomal vesicle | IEA | -- |
GO:0005794 | Golgi apparatus | IEA,IDA | 18218838 |
GO:0005829 | cytosol | IEA | -- |
GO:0012506 | vesicle membrane | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0007286 | spermatid development | IEA | -- |
GO:0009566 | fertilization | IEA | -- |
GO:0060009 | Sertoli cell development | IEA | -- |
GO:0098609 | cell-cell adhesion | IEA | -- |
This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | FNDC3A 30 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | FNDC3A 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | FNDC3A 30 31 |
|
OneToOne | |
Mouse (Mus musculus) |
Mammalia | Fndc3a 30 17 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | Fndc3a 30 |
|
||
Oppossum (Monodelphis domestica) |
Mammalia | FNDC3A 31 |
|
OneToOne | |
Platypus (Ornithorhynchus anatinus) |
Mammalia | FNDC3A 31 |
|
OneToOne | |
Chicken (Gallus gallus) |
Aves | FNDC3A 30 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | FNDC3A 31 |
|
OneToOne | |
Tropical Clawed Frog (Silurana tropicalis) |
Amphibia | LOC100492173 30 |
|
||
Str.15243 30 |
|
||||
African clawed frog (Xenopus laevis) |
Amphibia | Xl.21668 30 |
|
||
Zebrafish (Danio rerio) |
Actinopterygii | FNDC3A 31 |
|
OneToOne | |
Fruit Fly (Drosophila melanogaster) |
Insecta | CG42389 30 31 |
|
OneToMany | |
African malaria mosquito (Anopheles gambiae) |
Insecta | AgaP_AGAP009522 30 |
|
||
Worm (Caenorhabditis elegans) |
Secernentea | let-805 31 |
|
OneToMany | |
Sea Squirt (Ciona savignyi) |
Ascidiacea | -- 31 |
|
OneToMany |
SNP ID | Clinical significance and condition | Chr 13 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
768616 | Benign: not provided | 49,145,783(+) | C/T | NON_CODING_TRANSCRIPT_VARIANT,SYNONYMOUS_VARIANT | |
781263 | Benign: not provided | 49,186,098(+) | C/T | NON_CODING_TRANSCRIPT_VARIANT,SYNONYMOUS_VARIANT | |
785446 | Benign: not provided | 49,131,203(+) | A/G | MISSENSE_VARIANT,NON_CODING_TRANSCRIPT_VARIANT | |
rs34539036 | - | p.Ser107Gly |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
nsv1034 | CNV | deletion | 18451855 |
nsv1035 | CNV | deletion | 18451855 |
nsv1036 | CNV | insertion | 18451855 |
nsv1052168 | CNV | gain | 25217958 |
nsv1069751 | CNV | deletion | 25765185 |
nsv1126342 | CNV | deletion | 24896259 |
nsv455882 | CNV | loss | 19166990 |
nsv561593 | CNV | loss | 21841781 |
nsv832607 | CNV | loss | 17160897 |
nsv951081 | CNV | duplication | 24416366 |
Disorder | Aliases | PubMed IDs |
---|---|---|
deafness, autosomal dominant 56 |
|
|
deafness, autosomal recessive 100 |
|
|
deafness, autosomal recessive 97 |
|
|
epilepsy, familial adult myoclonic, 5 |
|
|
autism spectrum disorder |
|
|