KIAA0319
Sign in to saveAlso known as DYLX2, DYX2, NMIG
protein-coding gene in the species Homo sapiens
Gene data
KIAA0319- Name
- KIAA0319
- Type
- protein-coding
- Position
- 24,544,104–24,646,197 (−)
- Aliases
- DYLX2, DYX2, NMIG
- Ensembl
- ENSG00000137261
- RefSeq RNA
- NM_001168374.2, NM_001168375.2, NM_001168376.2, NM_001168377.2, NM_001252328.2
- RefSeq protein
- NP_001161846.1, NP_001161847.1, NP_001161848.1, NP_001161849.1, NP_001239257.1
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].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
KIAA0319
- Symbol
- KIAA0319
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 6:24,544,104-24,646,197
- Strand
- Reverse (−)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 8878
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/9856
- genomic end
- 24646191
- genomic start
- 24544332
- chromosome
- human chromosome 6
- cytogenetic location
- 6p22.3
Sources (3)
via Wikidata · CC0