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RNU6-77P RNA, U6 small nuclear 77, pseudogene [ Homo sapiens (human) ]

Gene ID: 106481792, updated on 10-Dec-2024

Summary

Official Symbol
RNU6-77Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 77, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:42567
See related
Ensembl:ENSG00000222486 AllianceGenome:HGNC:42567
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RNU6-77
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Genomic context

See RNU6-77P in Genome Data Viewer
Location:
13q31.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (81265747..81265837)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (80496162..80496252)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (81839882..81839972)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene DPPA3 pseudogene 3 Neighboring gene MPRA-validated peak2085 silencer Neighboring gene long intergenic non-protein coding RNA 564 Neighboring gene MPRA-validated peak2087 silencer Neighboring gene HIG1 hypoxia inducible domain family member 1A pseudogene 2 Neighboring gene uncharacterized LOC105370281

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_043924.1 

    Range
    101..191
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    81265747..81265837
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    80496162..80496252
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)