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SNORA101A small nucleolar RNA, H/ACA box 101A [ Homo sapiens (human) ]

Gene ID: 107399301, updated on 17-Sep-2024

Summary

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Official Symbol
SNORA101Aprovided by HGNC
Official Full Name
small nucleolar RNA, H/ACA box 101Aprovided by HGNC
Primary source
HGNC:HGNC:50405
See related
AllianceGenome:HGNC:50405
Gene type
snoRNA
RefSeq status
VALIDATED
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 SNORA101A in Genome Data Viewer
Location:
4q24
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (100395127..100395247, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (103710449..103710569, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (101316284..101316404, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107986232 Neighboring gene DDIT4L antisense RNA 1 Neighboring gene DNA damage inducible transcript 4 like Neighboring gene ReSE screen-validated silencer GRCh37_chr4:101170456-101170657 Neighboring gene uncharacterized LOC124900740 Neighboring gene endomucin Neighboring gene uncharacterized LOC105377345

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. snoStrip: a snoRNA annotation pipeline. Bartschat S, et al. Bioinformatics, 2014 Jan 1. PMID 24174566

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 Variation Viewer (GRCh37.p13)

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.

RNA

  1. NR_135619.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC097459

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    100395127..100395247 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    103710449..103710569 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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