SCARNA13 small Cajal body-specific RNA 13 [Homo sapiens (human)] - Gene

Summary

Official Symbol: SCARNA13provided by HGNC
Official Full Name: small Cajal body-specific RNA 13provided by HGNC
Primary source: HGNC:HGNC:32570
See related: Ensembl:ENSG00000252481 AllianceGenome:HGNC:32570
Gene type: ncRNA
RefSeq status: VALIDATED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: U93
Summary: Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

Location:: 14q32.13

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	14	NC_000014.9 (95533355..95533629, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	14	NC_060938.1 (89764048..89764322, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	14	NC_000014.8 (95999692..95999966, complement)

Chromosome 14 - NC_000014.9 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?

Domain specific mutations in dyskerin disrupt 3' end processing of scaRNA13.
Title: Domain specific mutations in dyskerin disrupt 3' end processing of scaRNA13.

Submit: New GeneRIF Correction

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)

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

RH98225 (e-PCR)
- UniSTS:89751

RH93740 (e-PCR)
- UniSTS:89752

Gene Ontology Provided by GOA

Process	Evidence Code	Pubs
involved_in RNA processing	IEA Inferred from Electronic Annotation more info

Component	Evidence Code	Pubs
located_in Cajal body	IMP Inferred from Mutant Phenotype more info	PubMed
located_in nucleolus	IEA Inferred from Electronic Annotation 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.