ADHDgene Database

Gene Report

Basic Info

Approved Symbol	INS-IGF2
Approved Name	INS-IGF2 readthrough
Location	11p15.5
Position	chr11:2150350-2182439, -
External Links	HGNC: 33527 UCSC: uc001lvm.2
No. of Studies	0 (significant: 0; non-significant: 0; trend: 0)
Source	Mapped by LD-proxy; Mapped by literature SNP

Gene related studies (count: 0)

Gene related SNPs (count: 4)

rs_ID	Location	Functional Annotation	No. of Studies (significant/non-significant/trend)
rs2070762	Chr11:2186335(Fwd)	downstream_gene_variant; intron_variant; upstream_gene_variant	2(1/1/0)
rs3842753	Chr11:2181060(Fwd)	3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; upstream_gene_variant	1(0/1/0)

rs_ID	Location	Functional Annotation
rs7924316	Chr11:2173447(Fwd)	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant
rs4320932	Chr11:2171601(Fwd)	NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant

Gene related CNVs (count: 0)

Gene related other variant (count: 0)

Gene related regions (count: 0)

Gene related GO terms (count: 0)

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with INS-IGF2 (count: 0)

Genes shared at least 2 KEGG pathways with INS-IGF2 (count: 0)

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Region: chr11:2150350..2182439 View in gBrowse