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

Gene ID: 101928731, updated on 25-Jan-2022

Summary

Official Symbol
CRADD-AS1provided by HGNC
Official Full Name
CRADD antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:56184
See related
Ensembl:ENSG00000258274
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
Biased expression in endometrium (RPKM 3.1), prostate (RPKM 1.0) and 5 other tissues See more
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Genomic context

See CRADD-AS1 in Genome Data Viewer
Location:
12q22
Exon count:
4
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 12 NC_000012.12 (93707791..93737823, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (94101567..94131599, complement)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene SOCS2 antisense RNA 1 Neighboring gene suppressor of cytokine signaling 2 Neighboring gene phosphoglycerate mutase 1 (brain) pseudogene Neighboring gene CASP2 and RIPK1 domain containing adaptor with death domain Neighboring gene Sharpr-MPRA regulatory region 9094 Neighboring gene RNA, 7SL, cytoplasmic 630, pseudogene

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

Phenotypes

EBI GWAS Catalog

Description
Hundreds of variants clustered in genomic loci and biological pathways affect human height.
EBI GWAS Catalog

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_110092.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AC012085, AC025261
    Related
    ENST00000550287.1
  2. NR_110093.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) contains an alternate last exon compared to variant 1.
    Source sequence(s)
    AC012085, AC025261

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_000012.12 Reference GRCh38.p13 Primary Assembly

    Range
    93707791..93737823 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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