SLC22A15
Homo sapiens
Gene Name: Solute carrier family 22, member 15
Aliases: UNQ9429/PRO34686, FLIPT1, PRO34686
Chromosome No: 1
Chromosome Band: 1p13.1
Genetic Category: Genetic association
Aliases: UNQ9429/PRO34686, FLIPT1, PRO34686
Chromosome No: 1
Chromosome Band: 1p13.1
Genetic Category: Genetic association
Summary Statistics:
ASD Reports: 1
Recent Reports: 0
Annotated variants: 1
Associated CNVs: 4
Evidence score: null
ASD Reports: 1
Recent Reports: 0
Annotated variants: 1
Associated CNVs: 4
Evidence score: null
| Associated Disorders: |
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Relevance to Autism
A SNP within the SLC22A15 gene showed association in the secondary analyses in a combined AGP GWA sample (Anney et al., 2012).
Molecular Function
Likely functions in the transport of organic cations.
External Links
References
Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
ASD