ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

Gene Report

Basic Info
Approved Symbol FMN1
Previous Symbol LD, FMN
Symbol Alias DKFZP686C2281, FLJ45135, MGC125288, MGC125289
Approved Name formin 1
Previous Name "formin (limb deformity)"
Name Alias "limb deformity protein"
Location 15q13.3
Position chr15:33057747-33486897, -1
External Links HGNC: 3768
Entrez Gene: 342184
Ensembl: ENSG00000248905
UCSC: uc031qrh.1
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source Mapped by CNV; Mapped by significant region

Gene related studies (count: 0)

Gene related SNPs (count: 0)

Gene related CNVs (count: 1)

Gene related other variant (count: 0)

Gene related regions (count: 2)

Gene related GO terms (count: 15)

GO terms by PBA (with statistical significance of FDR<0.05) (count: 0)

GO terms by database search (count: 15)

Gene related KEGG pathways (count: 0)

Genes shared at least 5 GO terms with FMN1 (count: 3)

Genes shared at least 2 KEGG pathways with FMN1 (count: 0)

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Region: chr15:33057747..33486897 View in gBrowse
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