RNY5 RNA, Ro60-associated Y5 [Homo sapiens (human)] - Gene

Summary

Official Symbol: RNY5provided by HGNC
Official Full Name: RNA, Ro60-associated Y5provided by HGNC
Primary source: HGNC:HGNC:10248
See related: MIM:601824; AllianceGenome:HGNC:10248
Gene type: ncRNA
RefSeq status: PROVISIONAL
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: Y5; hY5
Annotation information: Note: GeneID 6090 was incorrectly annotated on chromosome 12 on NCBI's Build 37.3. This gene is located at NT_007914.15:9234203 9234286 (+) in NCBI's build 37.3. [17 Jun 2014]
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Genomic context

Location:: 7q36.1

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	7	NC_000007.14 (148941488..148941571)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	7	NC_060931.1 (150123725..150123808)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	7	NC_000007.13 (148638580..148638663)

Chromosome 7 - NC_000007.14 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Y5 RNA uniquely copurified ribosomal protein L5 and its binding partner 5S RNA
Title: Human Y5 RNA specializes a Ro ribonucleoprotein for 5S ribosomal RNA quality control.

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Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

RNA, Ro-associated Y5
RNA, Y5 small cytoplasmic (associated with Ro protein)

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.