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RAP2C-AS1 RAP2C antisense RNA 1 [ Homo sapiens (human) ]

Gene ID: 101928578, updated on 12-Oct-2019

Summary

Official Symbol
RAP2C-AS1provided by HGNC
Official Full Name
RAP2C antisense RNA 1provided by HGNC
Primary source
HGNC:HGNC:40957
See related
Ensembl:ENSG00000232160
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
Ubiquitous expression in endometrium (RPKM 2.1), thyroid (RPKM 1.0) and 25 other tissues See more

Genomic context

See RAP2C-AS1 in Genome Data Viewer
Location:
Xq26.2
Exon count:
3
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (132218507..132432811)
105 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (131352650..131566380)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene serine/threonine kinase 26 Neighboring gene FERM domain containing 7 Neighboring gene acylglycerol kinase pseudogene Neighboring gene RAP2C, member of RAS oncogene family Neighboring gene muscleblind like splicing regulator 3 Neighboring gene RNA, U6 small nuclear 98, pseudogene Neighboring gene HS6ST2 antisense RNA 1 Neighboring gene heparan sulfate 6-O-sulfotransferase 2

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)

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_110410.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AK095439, CA867598
    Related
    ENST00000441399.3

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    132218507..132432811
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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