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Aliases for CLRN1-AS1 Gene

Subcategory (RNA class) for CLRN1-AS1 Gene

non-coding RNA

Quality Score for this RNA gene is


Aliases for CLRN1-AS1 Gene

  • CLRN1 Antisense RNA 1 2 3 5
  • CLRN1 Antisense RNA 1 (Non-Protein Coding) 2 3
  • Clarin 1 Opposite Strand 2 3
  • Usher Critical Region Protein Pseudogene 3
  • CLRN1OS 3
  • UCRP 3

External Ids for CLRN1-AS1 Gene

Previous HGNC Symbols for CLRN1-AS1 Gene


Previous GeneCards Identifiers for CLRN1-AS1 Gene

  • GC03P150571

Summaries for CLRN1-AS1 Gene

GeneCards Summary for CLRN1-AS1 Gene

CLRN1-AS1 (CLRN1 Antisense RNA 1) is an RNA Gene, and is affiliated with the non-coding RNA class. Diseases associated with CLRN1-AS1 include Retinitis Pigmentosa 61 and Usher Syndrome.

Gene Wiki entry for CLRN1-AS1 Gene

Additional gene information for CLRN1-AS1 Gene

No data available for Entrez Gene Summary , CIViC summary , UniProtKB/Swiss-Prot , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for CLRN1-AS1 Gene

Genomics for CLRN1-AS1 Gene

GeneHancer (GH) Regulatory Elements for CLRN1-AS1 Gene

Promoters and enhancers for CLRN1-AS1 Gene
GeneHancer (GH) Identifier GH Type GH
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH03J150888 Enhancer 0.7 Ensembl ENCODE 20.1 +37.6 37582 3.1 PKNOX1 HLF CEBPB CEBPG SPI1 ENSG00000243273 CLRN1-AS1 ERICH6-AS1 MED12L MINDY4B ENSG00000260234
GH03J151145 Enhancer 1.2 Ensembl ENCODE dbSUPER 10.5 +293.7 293723 1.7 RAD21 YY1 ZNF335 SCRT2 ZNF143 RCOR1 FOS DEK ZNF654 RXRA MED12L P2RY14 ENSG00000243273 MINDY4B CLRN1 CLRN1-AS1 GC03M151148
GH03J150925 Enhancer 1.1 FANTOM5 Ensembl ENCODE 11 +73.4 73385 0.9 CTCF KLF1 TFAP4 ZNF654 RNF2 SIN3A REST RAD21 XRCC5 CTBP1 MINDY4B ENSG00000243273 CLRN1 CLRN1-AS1 MED12L P2RY14 ENSG00000260234
GH03J151002 Enhancer 0.6 ENCODE 11 +150.7 150690 1.7 SOX13 GATAD2A JUND MAFF ZNF316 GLIS1 CREB1 SMAD4 BCL6 FOS MED12L CLRN1 CLRN1-AS1 MINDY4B ENSG00000243273 ENSG00000276055
GH03J151012 Enhancer 0.4 ENCODE 10.8 +162.4 162385 3.9 MXI1 MAX CLRN1 CLRN1-AS1 MED12L ENSG00000276055 ENSG00000243273
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around CLRN1-AS1 on UCSC Golden Path with GeneCards custom track

Genomic Locations for CLRN1-AS1 Gene

Genomic Locations for CLRN1-AS1 Gene
228,243 bases
Plus strand
228,243 bases
Plus strand

Genomic View for CLRN1-AS1 Gene

Genes around CLRN1-AS1 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
CLRN1-AS1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for CLRN1-AS1 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for CLRN1-AS1 Gene

Proteins for CLRN1-AS1 Gene

Post-translational modifications for CLRN1-AS1 Gene

No Post-translational modifications

No data available for DME Specific Peptides for CLRN1-AS1 Gene

Domains & Families for CLRN1-AS1 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 CLRN1-AS1 Gene

Function for CLRN1-AS1 Gene

Phenotypes From GWAS Catalog for CLRN1-AS1 Gene

Animal Model 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 CLRN1-AS1 Gene

Localization for CLRN1-AS1 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 CLRN1-AS1 Gene

Pathways & Interactions for CLRN1-AS1 Gene

SuperPathways for CLRN1-AS1 Gene

No Data Available

Interacting Proteins for CLRN1-AS1 Gene

Gene Ontology (GO) - Biological Process for CLRN1-AS1 Gene


No data available for Pathways by source and SIGNOR curated interactions for CLRN1-AS1 Gene

Drugs & Compounds for CLRN1-AS1 Gene

No Compound Related Data Available

Transcripts for CLRN1-AS1 Gene

mRNA/cDNA for CLRN1-AS1 Gene

(3) Additional mRNA sequences :
(2) Ensembl transcripts including schematic representations, and UCSC links where relevant :
(3) RNA Central transcripts :

Unigene Clusters for CLRN1-AS1 Gene

CLRN1 antisense RNA 1:
Representative Sequences:

Alternative Splicing Database (ASD) splice patterns (SP) for CLRN1-AS1 Gene

No ASD Table

Relevant External Links for CLRN1-AS1 Gene

GeneLoc Exon Structure for
ECgene alternative splicing isoforms for

Expression for CLRN1-AS1 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for CLRN1-AS1 Gene

mRNA differential expression in normal tissues according to GTEx for CLRN1-AS1 Gene

This gene is overexpressed in Whole Blood (x16.0), Liver (x4.9), and Uterus (x4.4).

SOURCE GeneReport for Unigene cluster for CLRN1-AS1 Gene:

genes like me logo Genes that share expression patterns with CLRN1-AS1: view

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , 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 CLRN1-AS1 Gene

Orthologs for CLRN1-AS1 Gene

Evolution for CLRN1-AS1 Gene

Gene Tree for CLRN1-AS1 (if available)
Gene Tree for CLRN1-AS1 (if available)

No data available for Orthologs for CLRN1-AS1 Gene

Paralogs for CLRN1-AS1 Gene

No data available for Paralogs for CLRN1-AS1 Gene

Variants for CLRN1-AS1 Gene

Sequence variations from dbSNP and Humsavar for CLRN1-AS1 Gene

SNP ID Clin Chr 03 pos Variation AA Info Type
rs1057517224 likely-pathogenic, Usher syndrome, type 3A 150,972,696(+) G/A/T non_coding_transcript_variant
rs111033258 pathogenic, uncertain-significance, likely-pathogenic, Usher syndrome, type 3A, Retinitis pigmentosa-deafness syndrome, Retinitis Pigmentosa, Dominant, not provided, Retinitis pigmentosa 150,972,565(+) A/C upstream_transcript_variant
rs111033267 pathogenic, Usher syndrome, type 3A, Retinitis pigmentosa 150,972,520(+) G/A/T upstream_transcript_variant
rs111033422 benign, not-provided, likely-benign, not specified, not provided, Retinitis Pigmentosa, Dominant, Retinitis pigmentosa-deafness syndrome 150,972,703(+) T/G non_coding_transcript_variant
rs111033434 likely-pathogenic, Usher syndrome, type 3A 150,972,582(+) C/T upstream_transcript_variant

Structural Variations from Database of Genomic Variants (DGV) for CLRN1-AS1 Gene

Variant ID Type Subtype PubMed ID
esv2656706 CNV deletion 23128226
esv2726047 CNV deletion 23290073
esv2726048 CNV deletion 23290073
esv2726049 CNV deletion 23290073
esv2726050 CNV deletion 23290073
esv2759188 CNV gain 17122850
esv2762349 CNV loss 21179565
esv3598168 CNV loss 21293372
nsv478908 CNV novel sequence insertion 20440878
nsv592045 CNV gain 21841781
nsv829756 CNV gain+loss 17160897

Additional Variant Information for CLRN1-AS1 Gene

SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot and Variation tolerance for CLRN1-AS1 Gene

Disorders for CLRN1-AS1 Gene

MalaCards: The human disease database

(3) MalaCards diseases for CLRN1-AS1 Gene - From: GeneCards

Disorder Aliases PubMed IDs
retinitis pigmentosa 61
  • rp61
usher syndrome
  • retinitis pigmentosa-deafness syndrome
retinitis pigmentosa
  • retinitis pigmentosa 1
- elite association - COSMIC cancer census association via MalaCards

Additional Disease Information for CLRN1-AS1

genes like me logo Genes that share disorders with CLRN1-AS1: view

No data available for UniProtKB/Swiss-Prot and Genatlas for CLRN1-AS1 Gene

Publications for CLRN1-AS1 Gene

  1. Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. (PMID: 11524702) Joensuu T … Sankila EM (American journal of human genetics 2001) 2 3 58
  2. Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. (PMID: 23382691) Lauc G … Rudan I (PLoS genetics 2013) 3 58
  3. Alternative splice variants of the USH3A gene Clarin 1 (CLRN1). (PMID: 20717163) Västinsalo H … Sankila EM (European journal of human genetics : EJHG 2011) 3 58
  4. Down-regulation of UCRP and UBE2L6 in BRCA2 knocked-down human breast cells. (PMID: 15670748) Tripathi MK … Chaudhuri G (Biochemical and biophysical research communications 2005) 22 58
  5. Complete sequencing and characterization of 21,243 full-length human cDNAs. (PMID: 14702039) Ota T … Sugano S (Nature genetics 2004) 3 58

Products for CLRN1-AS1 Gene

Sources for CLRN1-AS1 Gene

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