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CADM1-AS1 CADM1 antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 105369507, updated on 17-Jan-2022

Summary

Official Symbol
CADM1-AS1provided by HGNC
Official Full Name
CADM1 antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:56177
See related
Ensembl:ENSG00000256315
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
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Genomic context

See CADM1-AS1 in Genome Data Viewer
Location:
11q23.3
Exon count:
2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (115396756..115397658)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (115267474..115268376)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369506 Neighboring gene uncharacterized LOC105369505 Neighboring gene cell adhesion molecule 1 Neighboring gene uncharacterized LOC105369509 Neighboring gene uncharacterized LOC105369511 Neighboring gene ferritin light chain pseudogene 7

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

  1. NR_135102.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) uses an alternate splice site in the 3' exon resulting in a shorter transcript compared to variant 1.
    Source sequence(s)
    AA626163, AW082716, BX106383
    Related
    ENST00000543182.1
  2. NR_135103.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AA626163, AW082716, AW592507, BX106383

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    115396756..115397658
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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