SLC39A11
Homo sapiens
Gene Name: solute carrier family 39 member 11
Aliases: C17orf26, ZIP-11, ZIP11
Chromosome No: 17
Chromosome Band: 17q24.3-q25.1
Genetic Category: Genetic association-Rare single gene variant
Aliases: C17orf26, ZIP-11, ZIP11
Chromosome No: 17
Chromosome Band: 17q24.3-q25.1
Genetic Category: Genetic association-Rare single gene variant
Summary Statistics:
ASD Reports: 2
Recent Reports: 0
Annotated variants: 2
Associated CNVs: 9
Evidence score: 2
ASD Reports: 2
Recent Reports: 0
Annotated variants: 2
Associated CNVs: 9
Evidence score: 2
| Associated Disorders: |
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Relevance to Autism
A SNP within the SLC39A11 gene showed association in the secondary analyses in a combined AGP GWA sample (Anney et al., 2012).
Molecular Function
Belongs to the ZIP transporter family and may act as a zinc-influx transporter
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
Rare
Variant ID
Variant Type
Allele Change
Residue Change
Inheritance Pattern
Inheritance Association
Family Type
Author, Year
Common
Variant ID
Polymorphism
SNP ID
Allele Change
Residue Change
Population Origin
Population Stage
Author, Year
GEN402C001
intron_variant
rs9302952
c.147+16721T>G
Autism Genome Project (AGP)
Combined (Stages 1 and 2)
