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MIR29B2CHG MIR29B2 and MIR29C host gene [ Homo sapiens (human) ]

Gene ID: 100128537, updated on 23-Jul-2018

Summary

Official Symbol
MIR29B2CHGprovided by HGNC
Official Full Name
MIR29B2 and MIR29C host geneprovided by HGNC
Primary source
HGNC:HGNC:32018
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
C1orf132
Expression
Ubiquitous expression in fat (RPKM 4.1), adrenal (RPKM 3.4) and 24 other tissues See more

Genomic context

See MIR29B2CHG in Genome Data Viewer
Location:
1q32.2
Exon count:
6
Annotation release Status Assembly Chr Location
109 current GRCh38.p12 (GCF_000001405.38) 1 NC_000001.11 (207801518..207822703, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene complement C3b/C4b receptor 1 like Neighboring gene complement C3b/C4b receptor 1 (Knops blood group) pseudogene Neighboring gene cell division cycle associated 4 pseudogene 4 Neighboring gene CD46 molecule Neighboring gene microRNA 29b-2 Neighboring gene microRNA 29c Neighboring gene uncharacterized LOC148696 Neighboring gene uncharacterized LOC107985253 Neighboring gene CD34 molecule Neighboring gene uncharacterized LOC105372883

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000001.11 Chromosome 1 Reference GRCh38.p12 Primary Assembly

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

Bibliography

Related articles in PubMed

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Phenotypes

NHGRI GWAS Catalog

Description
Biological insights from 108 schizophrenia-associated genetic loci.
NHGRI GWA Catalog

General gene information

Markers

Clone Names

  • FLJ35650, FLJ41182

Gene Ontology Provided by GOA

Process Evidence Code Pubs
gene silencing by miRNA IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
micro-ribonucleoprotein complex IEA
Inferred from Electronic Annotation
more info
 

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_135298.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) represents the longer transcript.
    Source sequence(s)
    AA806730, EU154351
  2. NR_135299.1 RNA Sequence

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) contains an alternate internal exon, resulting in a longer transcript than variant 1.
    Source sequence(s)
    AA806730, EU154352

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

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

Reference GRCh38.p12 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p12 Primary Assembly

    Range
    207801518..207822703 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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