Leukodystrophy, hypomyelinating, 27

disease
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Summary

Leukodystrophy, hypomyelinating, 27 (MONDO:0958018) is a disease with 1 cohort gene.

At a glance

  • Cohort genes: 1
  • ClinVar variants: 10

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical nameleukodystrophy, hypomyelinating, 27
Mondo IDMONDO:0958018
OMIM620675
UMLSC5882743
MedGen1844996
GARD0026912
Is cancer (heuristic)no

Data availability: 10 ClinVar variants · 2 GenCC gene-disease records.

Disease family

Classification path: disease › human disease › disease by body system or component › nervous system disordercentral nervous system disorderneurodegenerative diseaseinherited neurodegenerative disorderleukodystrophyPOLR-related leukodystrophyleukodystrophy, hypomyelinating, 27

Related subtypes (1): POLR3-related leukodystrophy

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

ClinVar germline variants

10 retrieved; paginated sample, class counts are floors:

6 uncertain significance, 2 conflicting classifications of pathogenicity, 1 pathogenic, 1 likely pathogenic

ClinVarVariant (HGVS)GeneClassificationReview
3602728NM_015425.6(POLR1A):c.2357C>T (p.Thr786Ile)POLR1APathogeniccriteria provided, single submitter
4845757NM_015425.6(POLR1A):c.4297G>T (p.Glu1433Ter)POLR1ALikely pathogeniccriteria provided, single submitter
1395840NM_015425.6(POLR1A):c.4451G>A (p.Arg1484Gln)POLR1AConflicting classifications of pathogenicitycriteria provided, conflicting classifications
2778175NM_015425.6(POLR1A):c.978G>A (p.Val326=)POLR1AConflicting classifications of pathogenicitycriteria provided, conflicting classifications
1482607NM_015425.6(POLR1A):c.4330G>T (p.Asp1444Tyr)POLR1AUncertain significancecriteria provided, multiple submitters, no conflicts
2198814NM_015425.6(POLR1A):c.1031T>C (p.Leu344Ser)POLR1AUncertain significancecriteria provided, multiple submitters, no conflicts
3586944NM_015425.6(POLR1A):c.1463C>A (p.Pro488His)POLR1AUncertain significancecriteria provided, single submitter
3586945NM_015425.6(POLR1A):c.1380+4T>GPOLR1AUncertain significancecriteria provided, multiple submitters, no conflicts
3781702NM_015425.6(POLR1A):c.4708A>C (p.Asn1570His)POLR1AUncertain significancecriteria provided, multiple submitters, no conflicts
4818993NM_015425.6(POLR1A):c.1294A>G (p.Met432Val)POLR1AUncertain significancecriteria provided, single submitter

Genes & proteins

Mendelian disease overlap and somatic drivers

GenCC: 9 · Orphanet: 1 · OMIM-shared: 0 · Dual-evidence (GWAS+Mendelian): 0

GenCC gene–disease validity (cohort genes)

the Disease column is the GenCC-asserted condition — a cohort gene’s strongest validity may be for a related predisposition syndrome.

GeneClassificationInheritanceDiseaseRecords
POLR1AModerateAutosomal recessiveleukodystrophy, hypomyelinating, 279

Orphanet rare-disease linkage (cohort genes)

GeneOrphanet IDRare disease
POLR1AOrphanet:1200Burn-McKeown syndrome

Cohort genes → proteins

1 cohort genes, 1 distinct canonical proteins.

Evidence partition

SubsetGenes
multi_evidence1

Cohort genes (full)

SymbolHGNCEnsemblUniProtNameEvidence
POLR1AHGNC:17264ENSG00000068654O95602DNA-directed RNA polymerase I subunit RPA1gencc,clinvar

Cohort function summary

Lead sentence per gene, UniProt-curated.

SymbolProtein nameFunction (lead sentence)
POLR1ADNA-directed RNA polymerase I subunit RPA1Catalytic core component of RNA polymerase I (Pol I), a DNA-dependent RNA polymerase which synthesizes ribosomal RNA precursors using the four ribonucleoside triphosphates as substrates.

Protein-family classification

Druggable: 0 · Difficult: 0 · Unknown: 1 · Druggable fraction: 0.0

Family distribution

Cohort families vs a genome-wide background (hypergeometric, BH-FDR; fold = observed/expected). Counts kept; sorted by enrichment, so the catch-all Other/Unknown bucket no longer leads.

FamilyGenesFoldFDR
Other/Unknown11.8×0.558

Per-gene assignment

SymbolFamilyDruggable?ECInterPro (top 3)
POLR1AOther/UnknownnoRNA_pol_asu, RNA_pol_N, RNA_pol_Rpb1_3

Expression context

Cohort genes with no expression data: 0.

1 cohort gene are a single-cell marker in ≥1 SCXA experiment.

Breadth distribution (Bgee present_calls)

BucketGenes
narrow (1-5 tissues)0
moderate (6-20)0
broad (>20)1
unknown0

Top tissues across cohort

TissueCohort genes
stromal cell of endometrium1
sural nerve1
tibialis anterior1

Per-gene tissue summary (top 30)

SymbolBgee breadthFANTOM5 breadthSCXATop tissues
POLR1A198ubiquitousmarkersural nerve, tibialis anterior, stromal cell of endometrium

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

SymbolInteractor count
POLR1A4,620

Structural data

PDB: 1 · AlphaFold-only: 0 · No structure: 0

Cohort genes with PDB structures (top 30)

SymbolUniProtPDB entries
POLR1AO956027

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 11. Enrichment computed across 1 evidence-associated genes (1 with Reactome annotation).

Pathways by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

PathwayCohort genesFoldFDRSample cohort genes
Positive epigenetic regulation of rRNA expression1346.1×0.008POLR1A
RNA Polymerase I Transcription Termination1326.3×0.008POLR1A
RNA Polymerase I Promoter Clearance1292.8×0.008POLR1A
RNA Polymerase I Transcription1285.5×0.008POLR1A
Negative epigenetic regulation of rRNA expression1259.6×0.008POLR1A
RNA Polymerase I Transcription Initiation1223.9×0.008POLR1A
B-WICH complex positively regulates rRNA expression1121.5×0.011POLR1A
RNA Polymerase I Promoter Escape1121.5×0.011POLR1A
NoRC negatively regulates rRNA expression1104.8×0.012POLR1A
Epigenetic regulation of gene expression171.4×0.015POLR1A
Gene expression (Transcription)117.8×0.056POLR1A

GO biological processes by enrichment

Over-representation of cohort genes vs the genome-wide background (hypergeometric test, Benjamini-Hochberg FDR; fold = observed/expected over 1 annotated cohort genes). Counts and members are kept as ground-truth; sorted by enrichment.

GO termCohort genesFoldFDRSample cohort genes
negative regulation of protein localization to nucleolus15617.3×4e-04POLR1A
nucleolar large rRNA transcription by RNA polymerase I13370.4×4e-04POLR1A
transcription by RNA polymerase I11404.3×7e-04POLR1A

Therapeutics

Drug target analysis

Approved (phase 4): 0 · Phase ≥3: 0 · Phased (≥1): 1 · Undrugged: 0

Druggability breadth: 1 of 1 evidence-associated genes (100%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Top cohort targets by molecule count

SymbolMoleculesMax phase
POLR1A12

Drugs targeting cohort genes (top 30)

MoleculeMax phaseTargets in cohort
MOLIBRESIB2POLR1A

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

Cohort genes with ChEMBL bioactivity (full, sorted by assay count)

SymbolAssaysType breakdown
POLR1A16Binding:16

Pharmacogenomics

Cohort genes with a PharmGKB record: 1; with CPIC/DPWG dosing guidelines: 0.

No cohort gene has a CPIC/DPWG genotype-guided dosing guideline (PharmGKB).

Chemical tractability of cohort targets

1 approved/phased compounds have measured bioactivity against a cohort gene (and aren’t yet in disease-level trials). This is a research / tractability signal, NOT a therapeutic recommendation — a bioactivity row often reflects off-target or screening binding (e.g. promiscuous kinase inhibitors against a cohort kinase), implying no disease mechanism.

CompoundMax phaseCohort target (bioactivity)
MOLIBRESIB2POLR1A

Druggability pyramid

Cohort genes binned by druggability tier (high → low):

TierDefinitionGenesSymbols
AApproved (phase 4 drug)0
BPhased (≥1) drug, not yet approved1POLR1A
CDruggable family + PDB, no drug0
DDruggable family + AlphaFold only, no drug0
EDifficult family or no structure, no drug0

Undrugged target profiles

0 cohort genes are undrugged. Ranked by ‘starting-point quality’ (assay depth + drugged-partner adjacency).

Clinical trials & evidence

Clinical trials

Clinical trials: 0.