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SNURFL SNRPN upstream open reading frame like (pseudogene) [ Homo sapiens (human) ]

Gene ID: 727686, updated on 17-Jun-2024

Summary

Official Symbol
SNURFLprovided by HGNC
Official Full Name
SNRPN upstream open reading frame like (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:29543
See related
AllianceGenome:HGNC:29543
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
CXorf19
Summary
Predicted to be active in nuclear speck. [provided by Alliance of Genome Resources, Apr 2022]
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Genomic context

See SNURFL in Genome Data Viewer
Location:
Xq27.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (139361940..139362482)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (137671963..137672505)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (138444099..138444641)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene fibroblast growth factor 13 Neighboring gene tropomyosin 2 pseudogene Neighboring gene NFE2L2 motif-containing MPRA enhancer 215 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:138226529-138226732 Neighboring gene uncharacterized LOC124905222 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:138306638-138307247 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:138307248-138307856 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:138423703-138424360 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:138424361-138425018 Neighboring gene steroid 5 alpha-reductase 1 pseudogene 1 Neighboring gene coagulation factor IX

Genomic regions, transcripts, and products

General gene information

Other Names

  • SNRPN upstream reading frame like (pseudogene)

Gene Ontology Provided by GOA

Component Evidence Code Pubs
is_active_in nuclear speck IBA
Inferred from Biological aspect of Ancestor
more info
 

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_005696.2 

    Range
    101..643
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    139361940..139362482
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    137671963..137672505
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)