SNORA101B

Summary

SNORA101B (small nucleolar RNA, H/ACA box 101B, HGNC:50406) is a gene on chromosome 14q13.2.

Identifiers

Gene identifiers

Field	Value
HGNC ID	HGNC:50406
Approved symbol	SNORA101B
Name	small nucleolar RNA, H/ACA box 101B
Location	14q13.2
Locus type	RNA, small nucleolar
Status	Approved
Aliases	ZL4
Entrez	107399303
RNAcentral	URS0000ABD812 — snoRNA, 132 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): RS1000973776 (14:35763609 C>T), RS1002193015 (14:35763978 C>T), RS1002328974 (14:35764406 A>G), RS1004516573 (14:35764090 C>T), RS1005429742 (14:35764452 A>T), RS1005505420 (14:35762809 A>C), RS1005981437 (14:35764671 G>A), RS1008259 (14:35764173 C>G,T), RS1008588604 (14:35763514 TTTA>T), RS1009077205 (14:35763270 G>A), RS1009613753 (14:35763945 T>A), RS1010098277 (14:35763646 T>C), RS1013253559 (14:35762634 T>C), RS1013431523 (14:35762604 A>G), RS1013720542 (14:35762337 C>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: 0 entries

Clinical trials (associated diseases)

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