Gene Report

Basic Info
Approved Symbol FAM3C
Symbol Alias GS3876, ILEI
Approved Name family with sequence similarity 3, member C
Name Alias predicted osteoblast protein, "interleukin-like EMT inducer", "interleukin-like epithelial-mesenchymal transition inducer"
Location 7q22.1-q31.1
Position chr7:121348851-121396364, -1
External Links HGNC: 18664
Entrez Gene: 10447
Ensembl: ENSG00000196937
UCSC: uc010lkm.3
No. of Studies 1 (Positive: 1; Negative: 0; trend: 0)
Overlap with SZ? NO
Overlap with MDD? NO
Gene related studies (count: 1)
Reference Tested Markers Statistical Values/Author Comments Result Category Comment on Study
Chen, X., 2015 FAM3C has been implicated in Huntington disease, autism spectrum disorder and intellectual disability. Positive Comment on Study
Gene functional annotation
Gene related GO terms (count: 8)

GO terms by PBA (count: 2)

GO terms by database search (count: 6)

Gene related KEGG pathways (count: 0)

Gene related BioCarta pathways (count: 0)

Gene related interactors from protein-protein interactions data in HPRD (count: 0)

Related other genetic factors
Gene related SNPs (count: 0)

Gene related CNVs (count: 0)

Gene related other variants (count: 0)

Gene related regions (count: 5)

Overlap with schizophrenia (SZ) and major depressive disorder (MDD)
Gene relationship with SZ

Gene relationship with MDD

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Region: chr7:121348851..121396364 View in gBrowse
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