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This gene encodes a transmembrane protein that contains a large extracellular domain with multiple polycystic kidney disease (PKD) domains. The encoded protein may play a role in the development of the cerebral cortex by regulating neuronal migration and cell adhesion. Single nucleotide polymorphisms in this gene are associated with dyslexia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]
KIAA0319 (KIAA0319) is a Protein Coding gene. Diseases associated with KIAA0319 include Dyslexia 2 and Dyslexia. Among its related pathways are Clathrin-mediated endocytosis and Vesicle-mediated transport. Gene Ontology (GO) annotations related to this gene include calcium ion binding. An important paralog of this gene is KIAA0319L.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005515 | protein binding | IPI | 19419997 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005768 | endosome | IEA | -- |
GO:0005769 | early endosome | IDA | 19419997 |
GO:0005886 | plasma membrane | TAS | -- |
GO:0016020 | membrane | IEA | -- |
GO:0016021 | integral component of membrane | IEA | -- |
SuperPathway | Contained pathways | ||
---|---|---|---|
1 | Clathrin-mediated endocytosis | ||
2 | Vesicle-mediated transport |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0001764 | neuron migration | IBA,IGI | 19679544 |
GO:0007275 | multicellular organism development | IEA | -- |
GO:0007399 | nervous system development | IEA | -- |
GO:0010996 | response to auditory stimulus | IEA | -- |
GO:0030517 | negative regulation of axon extension | IMP | 28334068 |
ExUns: | 1 | ^ | 2a | · | 2b | · | 2c | ^ | 3 | ^ | 4a | · | 4b | · | 4c | · | 4d | ^ | 5 | ^ | 6 | ^ | 7 | ^ | 8 | ^ | 9 | ^ | 10 | ^ | 11 | ^ | 12 | ^ | 13 | ^ | 14 | ^ | 15 | ^ | 16 | ^ | 17 | ^ | 18 | ^ | 19 | ^ | 20 | ^ | 21 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | - | ||||||||||||||||||||||||||||||||||||||||||||||||||
SP2: | - | - | - | ||||||||||||||||||||||||||||||||||||||||||||||||
SP3: | |||||||||||||||||||||||||||||||||||||||||||||||||||
SP4: | - |
This gene was present in the common ancestor of animals.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | KIAA0319 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | KIAA0319 30 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | KIAA0319 30 31 |
|
OneToOne | |
Mouse (Mus musculus) |
Mammalia | D130043K22Rik 30 17 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | RGD1307443 30 |
|
||
Oppossum (Monodelphis domestica) |
Mammalia | KIAA0319 31 |
|
OneToOne | |
Chicken (Gallus gallus) |
Aves | KIAA0319 30 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | KIAA0319 31 |
|
OneToOne | |
Tropical Clawed Frog (Silurana tropicalis) |
Amphibia | kiaa0319 30 |
|
||
Zebrafish (Danio rerio) |
Actinopterygii | LOC794624 30 |
|
||
KIAA0319 31 |
|
OneToOne | |||
Fruit Fly (Drosophila melanogaster) |
Insecta | CG7565 30 31 32 |
|
OneToMany | |
African malaria mosquito (Anopheles gambiae) |
Insecta | AgaP_AGAP008639 30 |
|
||
Sea Squirt (Ciona savignyi) |
Ascidiacea | -- 31 |
|
OneToMany |
SNP ID | Clinical significance and condition | Chr 06 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
707909 | Benign: not provided | 24,556,708(-) | C/G | MISSENSE_VARIANT | |
714309 | Benign: not provided | 24,596,308(-) | G/A | SYNONYMOUS_VARIANT,INTRON_VARIANT | |
717701 | Likely Benign: not provided | 24,568,813(-) | C/T | MISSENSE_VARIANT | |
784065 | Benign: not provided | 24,576,557(-) | T/C | SYNONYMOUS_VARIANT,FIVE_PRIME_UTR_VARIANT | |
784066 | Benign: not provided | 24,579,869(-) | A/G | MISSENSE_VARIANT,FIVE_PRIME_UTR_VARIANT |
Disorder | Aliases | PubMed IDs |
---|---|---|
dyslexia 2 |
|
|
dyslexia |
|
|
reading disorder |
|
|
speech and communication disorders |
|
|
specific language impairment |
|
|