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RNU6-744P RNA, U6 small nuclear 744, pseudogene [ Homo sapiens (human) ]

Gene ID: 106479895, updated on 17-Sep-2024

Summary

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Official Symbol
RNU6-744Pprovided by HGNC
Official Full Name
RNA, U6 small nuclear 744, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:47707
See related
Ensembl:ENSG00000202427 AllianceGenome:HGNC:47707
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

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See RNU6-744P in Genome Data Viewer
Location:
2q14.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (113681112..113681214)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (114105844..114105946)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (114438689..114438791)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene SNRPA1 pseudogene 1 Neighboring gene ACR pseudogene 1 Neighboring gene long intergenic non-protein coding RNA 2936 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16422 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16423 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16424 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16425 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr2:114466525-114467155 Neighboring gene solute carrier family 35 member F5 Neighboring gene microRNA 4782 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 11886 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16426 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 16427 Neighboring gene uncharacterized LOC105373570 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:114575557-114576058 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:114576059-114576558

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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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_045018.1 

    Range
    101..203
    Download
    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    113681112..113681214
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    114105844..114105946
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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