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RNU6-1277P RNA, U6 small nuclear 1277, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480123, updated on 11-Sep-2019

Summary

Official Symbol
RNU6-1277Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1277, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48240
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See RNU6-1277P in Genome Data Viewer
Location:
14q21.1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 14 NC_000014.9 (37827798..37827904, complement)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene mirror-image polydactyly 1 Neighboring gene FOXA motif-containing MPRA enhancer 271 Neighboring gene forkhead box A1 Neighboring gene tetratricopeptide repeat domain 6 Neighboring gene long intergenic non-protein coding RNA 517 Neighboring gene uncharacterized LOC105370456

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000014.9 Chromosome 14 Reference GRCh38.p13 Primary Assembly

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.

Genomic

  1. NG_044900.1 

    Range
    101..207
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 details...Open this link in a new tab

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000014.9 Reference GRCh38.p13 Primary Assembly

    Range
    37827798..37827904 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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