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RNU6-137P RNA, U6 small nuclear 137, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481220, updated on 21-Mar-2023

Summary

Official Symbol
RNU6-137Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 137, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47100
See related
Ensembl:ENSG00000200550 AllianceGenome:HGNC:47100
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See RNU6-137P in Genome Data Viewer
Location:
2p21
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (42712740..42712847)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (42717993..42718100)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (42939880..42939987)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene metastasis associated 1 family member 3 Neighboring gene uncharacterized LOC105374555 Neighboring gene Sharpr-MPRA regulatory region 10188 Neighboring gene oxoeicosanoid receptor 1 Neighboring gene 3-hydroxyanthranilate 3,4-dioxygenase

Genomic regions, transcripts, and products

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.

Genomic

  1. NG_045057.1 

    Range
    101..208
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    42712740..42712847
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    42717993..42718100
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)