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Aliases for LOC107986257 Gene

Subcategory (RNA class) for LOC107986257 Gene

ncRNA

Quality Score for this RNA gene is

13

Aliases for LOC107986257 Gene

  • Uncharacterized LOC107986257 3

External Ids for LOC107986257 Gene

Summaries for LOC107986257 Gene

GeneCards Summary for LOC107986257 Gene

LOC107986257 (Uncharacterized LOC107986257) is an RNA Gene, and is affiliated with the ncRNA class. Diseases associated with LOC107986257 include Wfs1-Related Disorders and Wolfram-Like Syndrome, Autosomal Dominant.

Additional gene information for LOC107986257 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 LOC107986257 Gene

Genomics for LOC107986257 Gene

Genomic Locations for LOC107986257 Gene

Genomic Locations for LOC107986257 Gene
chr4:-
(GRCh38/hg38)
Orientation:
Unknown strand

Genomic View for LOC107986257 Gene


Cytogenetic band:
GeneLoc Logo Gene Density

RefSeq DNA sequence for LOC107986257 Gene

No data available for GeneHancer (GH) Regulatory Elements for LOC107986257 Gene

Proteins for LOC107986257 Gene

Post-translational modifications for LOC107986257 Gene

No Post-translational modifications

No data available for DME Specific Peptides for LOC107986257 Gene

Domains & Families for LOC107986257 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 LOC107986257 Gene

Function for LOC107986257 Gene

Phenotypes From GWAS Catalog for LOC107986257 Gene

Animal Model Products

Clone Products

No data available for Molecular function , Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , Human Phenotype Ontology , Animal Models , miRNA , Transcription Factor Targets and HOMER Transcription for LOC107986257 Gene

Localization for LOC107986257 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 LOC107986257 Gene

Pathways & Interactions for LOC107986257 Gene

SuperPathways for LOC107986257 Gene

No Data Available

Interacting Proteins for LOC107986257 Gene

Gene Ontology (GO) - Biological Process for LOC107986257 Gene

None

No data available for Pathways by source and SIGNOR curated interactions for LOC107986257 Gene

Drugs & Compounds for LOC107986257 Gene

No Compound Related Data Available

Transcripts for LOC107986257 Gene

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for LOC107986257 Gene

No ASD Table

No data available for mRNA/cDNA for LOC107986257 Gene

Expression for LOC107986257 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 LOC107986257 Gene

Orthologs for LOC107986257 Gene

No data available for Orthologs and Evolution for LOC107986257 Gene

Paralogs for LOC107986257 Gene

No data available for Paralogs for LOC107986257 Gene

Variants for LOC107986257 Gene

Sequence variations from dbSNP and Humsavar for LOC107986257 Gene

SNP ID Clin Chr 04 pos Variation AA Info Type
rs1007201071 uncertain-significance, WFS1-Related Spectrum Disorders, Nonsyndromic Hearing Loss, Dominant 6,302,974(-) C/T non_coding_transcript_variant
rs1046316 conflicting-interpretations-of-pathogenicity, benign, likely-benign, not specified, WFS1-Related Spectrum Disorders, Nonsyndromic Hearing Loss, Dominant 6,302,360(-) A/G/T downstream_transcript_variant
rs1046317 benign, WFS1-Related Spectrum Disorders, Nonsyndromic Hearing Loss, Dominant 6,302,515(-) T/C downstream_transcript_variant
rs1046319 benign, WFS1-Related Spectrum Disorders, Nonsyndromic Hearing Loss, Dominant 6,302,559(-) C/T downstream_transcript_variant
rs1046320 benign, Nonsyndromic Hearing Loss, Dominant, WFS1-Related Spectrum Disorders 6,302,617(-) G/A/T downstream_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 LOC107986257 Gene

Disorders for LOC107986257 Gene

MalaCards: The human disease database

(2) MalaCards diseases for LOC107986257 Gene - From: GeneCards

- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with LOC107986257: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for LOC107986257 Gene

Publications for LOC107986257 Gene

No publications were found for LOC107986257 Gene.

Products for LOC107986257 Gene

Sources for LOC107986257 Gene

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