SNORA100

Summary

SNORA100 (small nucleolar RNA, H/ACA box 100, HGNC:50404) is a gene on chromosome 1q44.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50404
Approved symbol	SNORA100
Name	small nucleolar RNA, H/ACA box 100
Location	1q44
Locus type	RNA, small nucleolar
Status	Approved
Entrez	106635532
RNAcentral	URS00008E395B — snoRNA, 131 nt, 1 organism(s)

Gene structure

Transcript identifiers

Ensembl transcripts: 0

RefSeq mRNA: 0 — MANE Select: None

Canonical transcript exons

None — 0 exons

Expression profiles

Top tissues by expression

0 total, by Bgee expression score (0-100, higher = more expressed):

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Canonical reviewed UniProt: None (reviewed: )

All UniProt accessions (0):

RefSeq proteins (0): (*=MANE)

Domains & families (InterPro)

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 0 (showing top):

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

Classification	Count (floor)
Pathogenic	0
Likely pathogenic	0
Uncertain significance	0
Likely benign	0
Benign	0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1001168123 (1:244854559 T>C), RS1002467737 (1:244853920 CTA>C), RS1003243084 (1:244854068 A>G), RS1004562963 (1:244855035 C>T), RS1006477158 (1:244855671 G>C), RS1009398044 (1:244854363 G>A), RS1009491514 (1:244853960 A>T), RS1011927428 (1:244854192 T>A,C), RS1013755447 (1:244856138 C>T), RS1013848842 (1:244855708 T>C), RS1017284922 (1:244854577 G>C,T), RS1017796381 (1:244853989 CAG>C), RS1020641922 (1:244853664 A>G), RS1020882404 (1:244853973 T>C), RS1020915119 (1:244854429 C>CA)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 0 entries

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.