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Aliases for LOC112268151 Gene

Subcategory (RNA class) for LOC112268151 Gene

ncRNA

Quality Score for this RNA gene is

13

Aliases for LOC112268151 Gene

  • Uncharacterized LOC112268151 3

External Ids for LOC112268151 Gene

Summaries for LOC112268151 Gene

GeneCards Summary for LOC112268151 Gene

LOC112268151 (Uncharacterized LOC112268151) is an RNA Gene, and is affiliated with the ncRNA class. Diseases associated with LOC112268151 include Epilepsy, Childhood Absence 5 and Epileptic Encephalopathy, Early Infantile, 43.

Additional gene information for LOC112268151 Gene

No data available for Entrez Gene Summary , CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for LOC112268151 Gene

Genomics for LOC112268151 Gene

Genomic Locations for LOC112268151 Gene

Genomic Locations for LOC112268151 Gene
chr15:-
(GRCh38/hg38)
Orientation:
Unknown strand

Genomic View for LOC112268151 Gene

RefSeq DNA sequence for LOC112268151 Gene

No data available for GeneHancer (GH) Regulatory Elements and Cytogenetic band for LOC112268151 Gene

Proteins for LOC112268151 Gene

Post-translational modifications for LOC112268151 Gene

No Post-translational modifications

No data available for DME Specific Peptides for LOC112268151 Gene

Domains & Families for LOC112268151 Gene

Graphical View of Domain Structure for InterPro Entry

No data available for Gene Families , Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for LOC112268151 Gene

Function for LOC112268151 Gene

Animal Model Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Phenotypes From GWAS Catalog , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for LOC112268151 Gene

Localization for LOC112268151 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS , Subcellular locations from the Human Protein Atlas (HPA) and Gene Ontology (GO) - Cellular Components for LOC112268151 Gene

Pathways & Interactions for LOC112268151 Gene

PathCards logo

SuperPathways for LOC112268151 Gene

No Data Available

Interacting Proteins for LOC112268151 Gene

Gene Ontology (GO) - Biological Process for LOC112268151 Gene

None

No data available for Pathways by source and SIGNOR curated interactions for LOC112268151 Gene

Drugs & Compounds for LOC112268151 Gene

No Compound Related Data Available

Transcripts for LOC112268151 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for LOC112268151 Gene

No ASD Table

No data available for mRNA/cDNA for LOC112268151 Gene

Expression for LOC112268151 Gene

No Expression Related Data Available

No data available for mRNA expression in normal human tissues , mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein differential expression in normal tissues , Protein expression , Protein tissue co-expression partners , mRNA Expression by UniProt/SwissProt , Evidence on tissue expression from TISSUES and Phenotype-based relationships between genes and organs from Gene ORGANizer for LOC112268151 Gene

Orthologs for LOC112268151 Gene

No data available for Orthologs and Evolution for LOC112268151 Gene

Paralogs for LOC112268151 Gene

No data available for Paralogs for LOC112268151 Gene

Variants for LOC112268151 Gene

Sequence variations from dbSNP and Humsavar for LOC112268151 Gene

SNP ID Clin Chr 15 pos Variation AA Info Type
rs1060504683 likely-benign, Epilepsy, childhood absence 1, Epilepsy, childhood absence 5 26,773,704(-) C/G/T upstream_transcript_variant
rs1064794797 likely-pathogenic, Epileptic encephalopathy, early infantile, 43, not provided 26,772,403(-) A/C/G upstream_transcript_variant
rs121913126 risk-factor, uncertain-significance, Epilepsy, childhood absence 5, not specified 26,773,681(-) G/A upstream_transcript_variant
rs1555383878 uncertain-significance, Epilepsy, childhood absence 1, Epilepsy, childhood absence 5 26,772,467(-) G/A upstream_transcript_variant
rs25409 uncertain-significance, benign-likely-benign, Epilepsy, childhood absence 5, not specified 26,773,694(-) G/A upstream_transcript_variant

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Structural Variations from Database of Genomic Variants (DGV) , Variation tolerance and Additional Variant Information for LOC112268151 Gene

Disorders for LOC112268151 Gene

MalaCards: The human disease database

(3) MalaCards diseases for LOC112268151 Gene - From: GeneCards

Disorder Aliases PubMed IDs
epilepsy, childhood absence 5
  • epilepsy, childhood absence, susceptibility to, 5
epileptic encephalopathy, early infantile, 43
  • eiee43
epilepsy, childhood absence 1
  • epilepsy, childhood absence, susceptibility to, 1
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with LOC112268151: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for LOC112268151 Gene

Publications for LOC112268151 Gene

No publications were found for LOC112268151 Gene.

No data available for External Links for LOC112268151 Gene

Products for LOC112268151 Gene

Sources for LOC112268151 Gene

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