FMC1-LUC7L2 (FMC1-LUC7L2 readthrough)

Gene Gene information from NCBI Gene database.
Gene Other IDs Associated diseases
Entrez ID 100996928
Gene name FMC1-LUC7L2 readthrough
Gene symbol FMC1-LUC7L2
Synonyms (NCBI Gene)
C7orf55C7orf55-LUC7L2FMC1
Chromosome 7
Chromosome location 7q34
Summary This locus represents naturally occurring readthrough transcription between the neighboring C7orf55 (chromosome 7 open reading frame 55) and LUC7L2 (LUC7-like 2) genes on chromosome 7. The readthrough transcript encodes a fusion protein that shares sequen
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene Other IDs Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Gene Other IDs Associated diseases
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Show/Hide Unknown Diseases (2)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ASTHMA — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
USHER SYNDROME — Disgenet
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (5)
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Asthma Asthma GWASCAT_DG 25918132
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Atherosclerotic Parkinsonism Atherosclerotic Parkinsonism CTD_human_DG 29371327
★★★★★
★☆☆☆☆
Found in Text Mining only
PARKINSON DISEASE, MITOCHONDRIAL (disorder) Parkinson Disease CTD_human_DG 29371327
★★★★★
★☆☆☆☆
Found in Text Mining only
Parkinson Disease, Secondary Vascular Parkinson Disease CTD_human_DG 29371327
★★★★★
★☆☆☆☆
Found in Text Mining only
Secondary Parkinson Disease Parkinson disease CTD_human_DG 29371327
★★★★★
★☆☆☆☆
Found in Text Mining only