Leukodystrophy, hypomyelinating, 27
disease diseaseOn this page
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
| Field | Value |
|---|---|
| Canonical name | leukodystrophy, hypomyelinating, 27 |
| Mondo ID | MONDO:0958018 |
| OMIM | 620675 |
| UMLS | C5882743 |
| MedGen | 1844996 |
| GARD | 0026912 |
| 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 disorder › central nervous system disorder › neurodegenerative disease › inherited neurodegenerative disorder › leukodystrophy › POLR-related leukodystrophy › leukodystrophy, 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
| ClinVar | Variant (HGVS) | Gene | Classification | Review |
|---|---|---|---|---|
| 3602728 | NM_015425.6(POLR1A):c.2357C>T (p.Thr786Ile) | POLR1A | Pathogenic | criteria provided, single submitter |
| 4845757 | NM_015425.6(POLR1A):c.4297G>T (p.Glu1433Ter) | POLR1A | Likely pathogenic | criteria provided, single submitter |
| 1395840 | NM_015425.6(POLR1A):c.4451G>A (p.Arg1484Gln) | POLR1A | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications |
| 2778175 | NM_015425.6(POLR1A):c.978G>A (p.Val326=) | POLR1A | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications |
| 1482607 | NM_015425.6(POLR1A):c.4330G>T (p.Asp1444Tyr) | POLR1A | Uncertain significance | criteria provided, multiple submitters, no conflicts |
| 2198814 | NM_015425.6(POLR1A):c.1031T>C (p.Leu344Ser) | POLR1A | Uncertain significance | criteria provided, multiple submitters, no conflicts |
| 3586944 | NM_015425.6(POLR1A):c.1463C>A (p.Pro488His) | POLR1A | Uncertain significance | criteria provided, single submitter |
| 3586945 | NM_015425.6(POLR1A):c.1380+4T>G | POLR1A | Uncertain significance | criteria provided, multiple submitters, no conflicts |
| 3781702 | NM_015425.6(POLR1A):c.4708A>C (p.Asn1570His) | POLR1A | Uncertain significance | criteria provided, multiple submitters, no conflicts |
| 4818993 | NM_015425.6(POLR1A):c.1294A>G (p.Met432Val) | POLR1A | Uncertain significance | criteria 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.
| Gene | Classification | Inheritance | Disease | Records |
|---|---|---|---|---|
| POLR1A | Moderate | Autosomal recessive | leukodystrophy, hypomyelinating, 27 | 9 |
Orphanet rare-disease linkage (cohort genes)
| Gene | Orphanet ID | Rare disease |
|---|---|---|
| POLR1A | Orphanet:1200 | Burn-McKeown syndrome |
Cohort genes → proteins
1 cohort genes, 1 distinct canonical proteins.
Evidence partition
| Subset | Genes |
|---|---|
| multi_evidence | 1 |
Cohort genes (full)
| Symbol | HGNC | Ensembl | UniProt | Name | Evidence |
|---|---|---|---|---|---|
| POLR1A | HGNC:17264 | ENSG00000068654 | O95602 | DNA-directed RNA polymerase I subunit RPA1 | gencc,clinvar |
Cohort function summary
Lead sentence per gene, UniProt-curated.
| Symbol | Protein name | Function (lead sentence) |
|---|---|---|
| POLR1A | DNA-directed RNA polymerase I subunit RPA1 | Catalytic 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.
| Family | Genes | Fold | FDR |
|---|---|---|---|
| Other/Unknown | 1 | 1.8× | 0.558 |
Per-gene assignment
| Symbol | Family | Druggable? | EC | InterPro (top 3) |
|---|---|---|---|---|
| POLR1A | Other/Unknown | no | RNA_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)
| Bucket | Genes |
|---|---|
| narrow (1-5 tissues) | 0 |
| moderate (6-20) | 0 |
| broad (>20) | 1 |
| unknown | 0 |
Top tissues across cohort
| Tissue | Cohort genes |
|---|---|
| stromal cell of endometrium | 1 |
| sural nerve | 1 |
| tibialis anterior | 1 |
Per-gene tissue summary (top 30)
| Symbol | Bgee breadth | FANTOM5 breadth | SCXA | Top tissues |
|---|---|---|---|---|
| POLR1A | 198 | ubiquitous | marker | sural nerve, tibialis anterior, stromal cell of endometrium |
Protein interactions among cohort
Intra-cohort edges: 0.
Hub genes (top 10 by interactor count)
| Symbol | Interactor count |
|---|---|
| POLR1A | 4,620 |
Structural data
PDB: 1 · AlphaFold-only: 0 · No structure: 0
Cohort genes with PDB structures (top 30)
| Symbol | UniProt | PDB entries |
|---|---|---|
| POLR1A | O95602 | 7 |
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.
| Pathway | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| Positive epigenetic regulation of rRNA expression | 1 | 346.1× | 0.008 | POLR1A |
| RNA Polymerase I Transcription Termination | 1 | 326.3× | 0.008 | POLR1A |
| RNA Polymerase I Promoter Clearance | 1 | 292.8× | 0.008 | POLR1A |
| RNA Polymerase I Transcription | 1 | 285.5× | 0.008 | POLR1A |
| Negative epigenetic regulation of rRNA expression | 1 | 259.6× | 0.008 | POLR1A |
| RNA Polymerase I Transcription Initiation | 1 | 223.9× | 0.008 | POLR1A |
| B-WICH complex positively regulates rRNA expression | 1 | 121.5× | 0.011 | POLR1A |
| RNA Polymerase I Promoter Escape | 1 | 121.5× | 0.011 | POLR1A |
| NoRC negatively regulates rRNA expression | 1 | 104.8× | 0.012 | POLR1A |
| Epigenetic regulation of gene expression | 1 | 71.4× | 0.015 | POLR1A |
| Gene expression (Transcription) | 1 | 17.8× | 0.056 | POLR1A |
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 term | Cohort genes | Fold | FDR | Sample cohort genes |
|---|---|---|---|---|
| negative regulation of protein localization to nucleolus | 1 | 5617.3× | 4e-04 | POLR1A |
| nucleolar large rRNA transcription by RNA polymerase I | 1 | 3370.4× | 4e-04 | POLR1A |
| transcription by RNA polymerase I | 1 | 1404.3× | 7e-04 | POLR1A |
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
| Symbol | Molecules | Max phase |
|---|---|---|
| POLR1A | 1 | 2 |
Drugs targeting cohort genes (top 30)
| Molecule | Max phase | Targets in cohort |
|---|---|---|
| MOLIBRESIB | 2 | POLR1A |
Bioactivity and enzyme data
Enzyme cohort genes (≥1 EC): 0.
Cohort genes with ChEMBL bioactivity (full, sorted by assay count)
| Symbol | Assays | Type breakdown |
|---|---|---|
| POLR1A | 16 | Binding: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.
| Compound | Max phase | Cohort target (bioactivity) |
|---|---|---|
| MOLIBRESIB | 2 | POLR1A |
Druggability pyramid
Cohort genes binned by druggability tier (high → low):
| Tier | Definition | Genes | Symbols |
|---|---|---|---|
| A | Approved (phase 4 drug) | 0 | |
| B | Phased (≥1) drug, not yet approved | 1 | POLR1A |
| C | Druggable family + PDB, no drug | 0 | |
| D | Druggable family + AlphaFold only, no drug | 0 | |
| E | Difficult family or no structure, no drug | 0 |
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.
Related Atlas pages
- Cohort genes: POLR1A