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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 transcript variant encodes a protein that shares sequence identity with the downstream gene product but its N-terminal region is shorter due to alternate exon use relative to the downstream gene. [provided by RefSeq, Dec 2016]
TNFAIP8L2-SCNM1 (TNFAIP8L2-SCNM1 Readthrough) is a Protein Coding gene.
GeneHancer (GH) Identifier | GH Type | GH Score |
GH Sources | Gene Association Score | Total Score | TSS distance (kb) | Number of Genes Away | Size (kb) | Transcription Factor Binding Sites |
Gene Targets |
---|---|---|---|---|---|---|---|---|---|---|
GH01J151156 | Promoter/Enhancer | 1.5 | EPDnew Ensembl ENCODE | 600.7 | +1.9 | 1933 | 4.9 | CREB1 CTCF ZNF512 POLR2A LARP7 PRDM1 REST RAD21 IKZF2 RCOR1 | SCNM1 TNFAIP8L2 TNFAIP8L2-SCNM1 SEMA6C BNIPL LYSMD1 | |
GH01J151164 | Promoter/Enhancer | 2.1 | EPDnew Ensembl ENCODE CraniofacialAtlas | 0.4 | +9.4 | 9356 | 3.2 | CEBPG SP1 CREB1 GATAD2A PRDM10 REST ZNF629 TFE3 RFX1 SIX5 | LYSMD1 NONHSAG002898.2 SCNM1 PRPF3 SETDB1 ARNT PI4KB CTSK UBE2D3P3 PIP5K1A | |
GH01J151165 | Enhancer | 0.3 | CraniofacialAtlas | 0.4 | +7.6 | 7576 | 0.2 | ZSCAN4 ZNF121 | LYSMD1 NONHSAG002898.2 SCNM1 TNFAIP8L2-SCNM1 | |
GH01J151153 | Enhancer | 0.2 | Ensembl | 0.7 | -2.7 | -2748 | 0.2 | lnc-SEMA6C-2 TNFAIP8L2 TNFAIP8L2-SCNM1 SEMA6C LYSMD1 |
SNP ID | Clinical significance and condition | Chr 01 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
708675 | Benign: not provided | 151,159,105(+) | G/A | SYNONYMOUS_VARIANT,INTRON_VARIANT | |
723112 | Benign: not provided | 151,158,768(+) | G/A | MISSENSE_VARIANT,INTRON_VARIANT | |
775139 | Benign: not provided | 151,159,060(+) | C/G | SYNONYMOUS_VARIANT,INTRON_VARIANT |
No disorders were found for TNFAIP8L2-SCNM1 Gene.