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Aliases for LOC105371567 Gene

Subcategory (RNA class) for LOC105371567 Gene

ncRNA

Quality Score for this RNA gene is

13

Aliases for LOC105371567 Gene

  • Uncharacterized LOC105371567 3

External Ids for LOC105371567 Gene

Summaries for LOC105371567 Gene

GeneCards Summary for LOC105371567 Gene

LOC105371567 (Uncharacterized LOC105371567) is an RNA Gene, and is affiliated with the ncRNA class. Diseases associated with LOC105371567 include Deafness, Autosomal Recessive 3.

Additional gene information for LOC105371567 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 LOC105371567 Gene

Genomics for LOC105371567 Gene

Genomic Locations for LOC105371567 Gene

Genomic Locations for LOC105371567 Gene
chr17:-
(GRCh38/hg38)
Orientation:
Unknown strand

Genomic View for LOC105371567 Gene


Cytogenetic band:
GeneLoc Logo Gene Density

RefSeq DNA sequence for LOC105371567 Gene

No data available for GeneHancer (GH) Regulatory Elements for LOC105371567 Gene

Proteins for LOC105371567 Gene

Post-translational modifications for LOC105371567 Gene

No Post-translational modifications

No data available for DME Specific Peptides for LOC105371567 Gene

Domains & Families for LOC105371567 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 LOC105371567 Gene

Function for LOC105371567 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 LOC105371567 Gene

Localization for LOC105371567 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 LOC105371567 Gene

Pathways & Interactions for LOC105371567 Gene

PathCards logo

SuperPathways for LOC105371567 Gene

No Data Available

Interacting Proteins for LOC105371567 Gene

Gene Ontology (GO) - Biological Process for LOC105371567 Gene

None

No data available for Pathways by source and SIGNOR curated interactions for LOC105371567 Gene

Drugs & Compounds for LOC105371567 Gene

No Compound Related Data Available

Transcripts for LOC105371567 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for LOC105371567 Gene

No ASD Table

No data available for mRNA/cDNA for LOC105371567 Gene

Expression for LOC105371567 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 LOC105371567 Gene

Orthologs for LOC105371567 Gene

No data available for Orthologs and Evolution for LOC105371567 Gene

Paralogs for LOC105371567 Gene

No data available for Paralogs for LOC105371567 Gene

Variants for LOC105371567 Gene

Sequence variations from dbSNP and Humsavar for LOC105371567 Gene

SNP ID Clin Chr 17 pos Variation AA Info Type
rs1006770 benign, uncertain-significance, not specified, Nonsyndromic Hearing Loss, Recessive 18,155,147(-) G/A intron_variant
rs1057519605 uncertain-significance, Deafness, autosomal recessive 3 18,154,758(-) A/G intron_variant
rs121908969 pathogenic, Deafness, autosomal recessive 3 18,154,190(-) G/T non_coding_transcript_variant
rs140140417 benign-likely-benign, uncertain-significance, not specified, Nonsyndromic Hearing Loss, Recessive 18,155,154(-) G/A intron_variant
rs181229675 uncertain-significance, Nonsyndromic Hearing Loss, Recessive 18,155,404(-) G/A/C 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 LOC105371567 Gene

Disorders for LOC105371567 Gene

MalaCards: The human disease database

(1) MalaCards diseases for LOC105371567 Gene - From: GeneCards

Disorder Aliases PubMed IDs
deafness, autosomal recessive 3
  • dfnb3
- elite association - COSMIC cancer census association via MalaCards
genes like me logo Genes that share disorders with LOC105371567: view

No data available for UniProtKB/Swiss-Prot , Genatlas and External Links for LOC105371567 Gene

Publications for LOC105371567 Gene

No publications were found for LOC105371567 Gene.

No data available for External Links for LOC105371567 Gene

Products for LOC105371567 Gene

Sources for LOC105371567 Gene

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