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LOC105378311 (Uncharacterized LOC105378311) is an RNA Gene, and is affiliated with the lncRNA class. Diseases associated with LOC105378311 include Deafness, Autosomal Recessive 23 and Usher Syndrome.
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 |
---|---|---|---|---|---|---|---|---|---|---|
GH10J054478 | Enhancer | 0.2 | Ensembl | 0.4 | -7.5 | -7529 | 0.6 | LOC105378311 RNU6-687P | ||
GH10J054474 | Enhancer | 0.2 | Ensembl | 0.4 | -11.6 | -11629 | 0.4 | LOC105378311 RNU6-687P | ||
GH10J054613 | Enhancer | 0.5 | Ensembl | 0.1 | +127.3 | 127271 | 1.8 | NFE2 ZNF316 MAFF MAFK MAFG NFE2L2 JUN | MIR548F1 piR-37698-001 LOC105378311 MTRNR2L5 | |
GH10J054585 | Enhancer | 0.3 | Ensembl | 0.2 | +99.6 | 99571 | 0.4 | CHD2 | NEFMP1 piR-46002-062 LOC105378311 | |
GH10J054587 | Enhancer | 0.3 | Ensembl | 0.1 | +102.1 | 102071 | 1 | JUN | NEFMP1 piR-46002-062 LOC105378311 |
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS000034C6E0_9606 | lncRNA | 2300 | 2 |
Ensembl: ENST00000422842 (view in UCSC) , LNCipedia: lnc-MTRNR2L5-4:1, |
URS0000A768E8_9606 | lncRNA | 2300 | 1 |
RefSeq: NR_134503, |
URS00008BEABA_9606 | lncRNA | 2305 | 3 |
LncBook: HSALNT0162925, LNCipedia: lnc-MTRNR2L5-4:2, NONCODE: NONHSAT013457.2, |
SNP ID | Clinical significance and condition | Chr 10 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
691400 | Uncertain Significance: Hirschsprung disease | 54,527,830(+) | C/T | MISSENSE_VARIANT,INTRON_VARIANT | |
793999 | Likely Benign: not provided | 54,528,378(+) | G/A | INTRON_VARIANT | |
797799 | Likely Benign: not provided | 54,527,876(+) | A/G | SYNONYMOUS_VARIANT,INTRON_VARIANT | |
880274 | Uncertain Significance: Usher syndrome type 1 | 54,527,823(+) | T/C | MISSENSE_VARIANT,INTRON_VARIANT | |
rs1057516770 | Likely Pathogenic: Usher syndrome type 1F | 54,527,811(+) | C/G | SPLICE_DONOR_VARIANT,INTRON_VARIANT |
Disorder | Aliases | PubMed IDs |
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deafness, autosomal recessive 23 |
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usher syndrome |
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