Gene Gene information from NCBI Gene database.
Entrez ID 100534012
Gene name -
Gene symbol TNFAIP8L2-SCNM1
Synonyms (NCBI Gene)
SCNM1
Chromosome 1
Chromosome location 1q21.3
Summary This locus represents naturally occurring read-through transcription between the neighboring TNFAIP8L2 (tumor necrosis factor, alpha-induced protein 8-like 2) and SCNM1 (sodium channel modifier 1) genes on chromosome 1. The protein-coding read-through tra
miRNA miRNA information provided by mirtarbase database.
293
miRTarBase ID miRNA Experiments Reference
MIRT1442452 hsa-miR-1207-5p CLIP-seq
MIRT1442453 hsa-miR-1285 CLIP-seq
MIRT1442454 hsa-miR-1321 CLIP-seq
MIRT1442455 hsa-miR-146b-3p CLIP-seq
MIRT1442456 hsa-miR-1827 CLIP-seq
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
ENSG00000163156 N/A N/A
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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)
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
OROFACIODIGITAL SYNDROME XIX Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Dystonia Disorders Dystonia BEFREE 9949206
★☆☆☆☆
Found in Text Mining only
nervous system disorder Nervous System Disorder BEFREE 13679025
★☆☆☆☆
Found in Text Mining only
Orofaciodigital Syndromes Orofaciodigital syndrome Pubtator 36084634 Associate
★☆☆☆☆
Found in Text Mining only