C1QTNF5 Chromosome 11

C1q and TNF related 5
9 variants 9 Health Risk

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What This Gene Does
This gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late-onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled-related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter. [provided by RefSeq, Jun 2013]
Gene Info
Gene Group
C1q and TNF related
Locus Type
gene with protein product
Location
11q23.3
Ensembl
ENSG00000223953
Associated Conditions (3)
Retinal dystrophy
C1QTNF5-related disorder
Late-onset retinal degeneration
Key Variants
All Variants (9)
RSID Category Clinical Significance Conditions
RS143241967 Health Risk Conflicting classifications of pathogenicity —
RS1950474024 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS751346951 Health Risk Conflicting classifications of pathogenicity C1QTNF5-related disorder, C1QTNF5-related disorder
RS760578346 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS883246 Health Risk Conflicting classifications of pathogenicity —
RS1555036138 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS906525288 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
RS111033578 Health Risk Pathogenic/Likely pathogenic Late-onset retinal degeneration, Retinal dystrophy, Retinal dystrophy
RS1591299252 Health Risk Pathogenic/Likely pathogenic Late-onset retinal degeneration, Late-onset retinal degeneration, Retinal dystrophy
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