SNORD103B

Summary

SNORD103B (small nucleolar RNA, C/D box 103B, HGNC:32767) is a gene on chromosome 1p35.2.

Predicted to be involved in RNA processing. Predicted to be located in nucleolus.

Source: NCBI Gene 692235 — RefSeq curated summary.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:32767
Approved symbol	SNORD103B
Name	small nucleolar RNA, C/D box 103B
Location	1p35.2
Locus type	RNA, small nucleolar
Status	Approved
Aliases	U103B
Entrez	692235
RNAcentral	URS000075CFA2 — snoRNA, 88 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): RS1003204825 (1:30949526 G>A), RS1003615361 (1:30950955 T>C), RS1005716106 (1:30948863 T>A), RS1006081089 (1:30949390 G>A), RS1007401771 (1:30950395 T>C,G), RS1007804104 (1:30950600 C>T), RS1010573508 (1:30949782 G>A), RS1010912510 (1:30949843 C>T), RS1010987060 (1:30949993 T>C,G), RS1011471177 (1:30949566 T>A), RS1012478781 (1:30950982 T>C), RS1017546151 (1:30948885 T>C), RS1017763914 (1:30950400 T>C,G), RS1018128930 (1:30950460 T>C), RS1021516159 (1:30949845 T>A)

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: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

Chemical	Actions (top 5)	PubMed papers
bisphenol A	affects expression	1

Clinical trials (associated diseases)

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