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
- Aliases
- DYLX2, DYX2, NMIG
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].
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
Show 5 more facts
- HomoloGene ID
- 8878
- exact match
- identifiers.org/ncbigene/9856
- genomic end
- 24646191
- genomic start
- 24544332
- cytogenetic location
- 6p22.3
Sources (3)
via Wikidata · CC0
Connections
Q180686
Entity
human chromosome 6
Entity
Ensembl genome database project
Entity
protein
Entity
Wikidata
Entity
gene
Entity
chromosome
Entity
digital object identifier
Entity
dyslexia
Entity
plasma membrane
Entity
bibcode
Entity
human genome
Entity
Q229883
Entity
base pair
Entity
locus
Entity
gene expression
Entity
endocytosis
Entity
Online Mendelian Inheritance in Man
Entity
Protein Data Bank
Entity
Q22908627
Entity