Format

Send to:

Choose Destination

RNU6-1293P RNA, U6 small nuclear 1293, pseudogene [ Homo sapiens (human) ]

Gene ID: 106480130, updated on 12-Oct-2019

Summary

Official Symbol
RNU6-1293Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 1293, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:48256
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 RNU6-1293P in Genome Data Viewer
Location:
9q13
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 9 NC_000009.12 (64880369..64880475, complement)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene ankyrin repeat domain 30B pseudogene Neighboring gene ZFP37 zinc finger protein pseudogene Neighboring gene vomeronasal 1 receptor 49 pseudogene Neighboring gene uncharacterized LOC102724507 Neighboring gene methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like pseudogene Neighboring gene BMS1 pseudogene 12

Genomic regions, transcripts, and products

Genomic Sequence:
NC_000009.12 Chromosome 9 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_042915.1 

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

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_000009.12 Reference GRCh38.p13 Primary Assembly

    Range
    64880369..64880475 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Support Center