Autosomal dominant nonsyndromic hearing loss 44

Summary

Autosomal dominant nonsyndromic hearing loss 44 (MONDO:0011832) is a disease with 1 cohort gene.

At a glance

• Cohort genes: 1
• ClinVar variants: 20

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

Field	Value
Canonical name	autosomal dominant nonsyndromic hearing loss 44
Mondo ID	MONDO:0011832
MeSH	C564399
OMIM	607453
DOID	DOID:0110569
UMLS	C1843895
MedGen	334525
GARD	0018118
Is cancer (heuristic)	no

Also known as: autosomal dominant deafness 44 · autosomal dominant nonsyndromic deafness 44 · autosomal dominant nonsyndromic deafness caused by mutation in CCDC50 · autosomal dominant nonsyndromic deafness type 44 · CCDC50 autosomal dominant nonsyndromic deafness · deafness, autosomal dominant 44 · deafness, autosomal dominant type 44 · DFNA44

Data availability: 20 ClinVar variants · 2 GenCC gene-disease records.

Disease family

Classification path: disease › human disease › disease by etiologic mechanism › disease of genetic or genomic mechanism › hereditary disease › autosomal genetic disease › autosomal dominant disease › autosomal dominant nonsyndromic hearing loss › autosomal dominant nonsyndromic hearing loss 44

Related subtypes (75): autosomal dominant nonsyndromic hearing loss 1, autosomal dominant nonsyndromic hearing loss 2A, autosomal dominant nonsyndromic hearing loss 4A, autosomal dominant nonsyndromic hearing loss 6, autosomal dominant nonsyndromic hearing loss 5, autosomal dominant nonsyndromic hearing loss 10, autosomal dominant nonsyndromic hearing loss 11, autosomal dominant nonsyndromic hearing loss 9, autosomal dominant nonsyndromic hearing loss 7, autosomal dominant nonsyndromic hearing loss 12, autosomal dominant nonsyndromic hearing loss 3A, autosomal dominant nonsyndromic hearing loss 13, autosomal dominant nonsyndromic hearing loss 15, autosomal dominant nonsyndromic hearing loss 17, autosomal dominant nonsyndromic hearing loss 16, autosomal dominant nonsyndromic hearing loss 20, autosomal dominant nonsyndromic hearing loss 23, autosomal dominant nonsyndromic hearing loss 25, autosomal dominant nonsyndromic hearing loss 18, autosomal dominant nonsyndromic hearing loss 24, autosomal dominant nonsyndromic hearing loss 22, autosomal dominant nonsyndromic hearing loss 30, autosomal dominant nonsyndromic hearing loss 36, autosomal dominant nonsyndromic hearing loss 21, autosomal dominant nonsyndromic hearing loss 48, autosomal dominant nonsyndromic hearing loss 41, autosomal dominant nonsyndromic hearing loss 49, autosomal dominant nonsyndromic hearing loss 43, autosomal dominant nonsyndromic hearing loss 28, autosomal dominant nonsyndromic hearing loss 31, autosomal dominant nonsyndromic hearing loss 47, autosomal dominant auditory neuropathy 1, autosomal dominant nonsyndromic hearing loss 53, autosomal dominant nonsyndromic hearing loss 27, autosomal dominant nonsyndromic hearing loss 59, autosomal dominant nonsyndromic hearing loss 3B, autosomal dominant nonsyndromic hearing loss 2B, autosomal dominant nonsyndromic hearing loss 50, autosomal dominant nonsyndromic hearing loss 51, autosomal dominant nonsyndromic hearing loss 64, autosomal dominant nonsyndromic hearing loss 33, autosomal dominant nonsyndromic hearing loss 4B, autosomal dominant nonsyndromic hearing loss 56, autosomal dominant nonsyndromic hearing loss 54, autosomal dominant nonsyndromic hearing loss 58, autosomal dominant nonsyndromic hearing loss 65, autosomal dominant nonsyndromic hearing loss 67, autosomal dominant nonsyndromic hearing loss 40, autosomal dominant nonsyndromic hearing loss 69, autosomal dominant nonsyndromic hearing loss 68, autosomal dominant nonsyndromic hearing loss 70, autosomal dominant nonsyndromic hearing loss 66, hearing loss, autosomal dominant 74, hearing loss, autosomal dominant 77, hearing loss, autosomal dominant 81, hearing loss, autosomal dominant 82, hearing loss, autosomal dominant 83, hearing loss, autosomal dominant 84, hearing loss, autosomal dominant 80, hearing loss, autosomal dominant 37, hearing loss, autosomal dominant 75, hearing loss, autosomal dominant 76, hearing loss, autosomal dominant 71, hearing loss, autosomal dominant 72, hearing loss, autosomal dominant 73, hearing loss, autosomal dominant 34, with or without inflammation, hearing loss, autosomal dominant 78, hearing loss, autosomal dominant 79, hearing loss, autosomal dominant 85, hearing loss, autosomal dominant 86, hearing loss, autosomal dominant 87, hearing loss, autosomal dominant 88, hearing loss, autosomal dominant 89, hearing loss, autosomal dominant 90, autosomal dominant nonsyndromic hearing loss 91

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

20 retrieved; paginated sample, class counts are floors:

11 benign, 5 uncertain significance, 1 no classifications from unflagged records, 1 pathogenic, 1 conflicting classifications of pathogenicity, 1 likely pathogenic

ClinVar	Variant (HGVS)	Gene	Classification	Review
1330217	NM_178335.3(CCDC50):c.1356_1386del (p.Asp452fs)	CCDC50	Pathogenic	criteria provided, single submitter
3572930	NM_178335.3(CCDC50):c.802C>T (p.Gln268Ter)	CCDC50	Likely pathogenic	criteria provided, single submitter
1376607	NM_178335.3(CCDC50):c.227G>A (p.Arg76His)	CCDC50	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications
1032557	NM_178335.3(CCDC50):c.199C>G (p.Leu67Val)	CCDC50	Uncertain significance	criteria provided, single submitter
1036	NM_178335.3(CCDC50):c.1394_1401dup (p.Phe468fs)	CCDC50	no classifications from unflagged records	no classifications from unflagged records
1185117	NM_178335.3(CCDC50):c.679C>T (p.Arg227Trp)	CCDC50	Uncertain significance	criteria provided, multiple submitters, no conflicts
1805828	NM_178335.3(CCDC50):c.372G>C (p.Glu124Asp)	CCDC50	Uncertain significance	criteria provided, single submitter
3027427	NM_178335.3(CCDC50):c.1105G>T (p.Asp369Tyr)	CCDC50	Uncertain significance	criteria provided, single submitter
4292779	NM_178335.3(CCDC50):c.50-851T>G	CCDC50	Uncertain significance	criteria provided, single submitter
1178730	NM_178335.3(CCDC50):c.1092+58C>T	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
1192702	NM_178335.3(CCDC50):c.976+56A>G	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
162857	NM_178335.3(CCDC50):c.883G>T (p.Asp295Tyr)	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48150	NM_178335.3(CCDC50):c.1242+10G>A	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48151	NM_178335.3(CCDC50):c.1269C>A (p.Ser423=)	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48155	NM_178335.3(CCDC50):c.50-4C>G	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48156	NM_178335.3(CCDC50):c.651T>C (p.His217=)	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48158	NM_178335.3(CCDC50):c.773T>A (p.Ile258Asn)	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48159	NM_178335.3(CCDC50):c.908A>G (p.Lys303Arg)	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48160	NM_178335.3(CCDC50):c.976+6A>G	CCDC50	Benign	criteria provided, multiple submitters, no conflicts
48161	NM_178335.3(CCDC50):c.995T>C (p.Met332Thr)	CCDC50	Benign	criteria provided, multiple submitters, no conflicts

Genes & proteins

Mendelian disease overlap and somatic drivers

GenCC: 4 · 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
CCDC50	Supportive	Autosomal dominant	autosomal dominant nonsyndromic hearing loss	4

Orphanet rare-disease linkage (cohort genes)

Gene	Orphanet ID	Rare disease
CCDC50	Orphanet:90635	Rare autosomal dominant non-syndromic sensorineural deafness type DFNA

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
CCDC50	HGNC:18111	ENSG00000152492	Q8IVM0	Coiled-coil domain-containing protein 50	gencc,clinvar

Cohort function summary

Lead sentence per gene, UniProt-curated.

Symbol	Protein name	Function (lead sentence)
CCDC50	Coiled-coil domain-containing protein 50	Involved in EGFR signaling.

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)
CCDC50	Other/Unknown	no		CCDC50_N, CCDC50

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
calcaneal tendon	1
ileal mucosa	1
oviduct epithelium	1

Per-gene tissue summary (top 30)

Symbol	Bgee breadth	FANTOM5 breadth	SCXA	Top tissues
CCDC50	256	ubiquitous	marker	oviduct epithelium, ileal mucosa, calcaneal tendon

Protein interactions among cohort

Intra-cohort edges: 0.

Hub genes (top 10 by interactor count)

Symbol	Interactor count
CCDC50	154

Structural data

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

Cohort genes with PDB structures (top 30)

Symbol	UniProt	PDB entries
CCDC50	Q8IVM0	1

Function

Pathway analysis

Distinct Reactome pathways touched by cohort: 0. Enrichment computed across 1 evidence-associated genes (0 with Reactome annotation).

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
sensory perception of sound	1	100.9×	0.010	CCDC50

Therapeutics

Drug target analysis

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

Druggability breadth: 0 of 1 evidence-associated genes (0%) have a ChEMBL target (buckets above are over the deeply-mined display cohort).

Top cohort targets by molecule count

Symbol	Molecules	Max phase
CCDC50	0	0

Bioactivity and enzyme data

Enzyme cohort genes (≥1 EC): 0.

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

0 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.

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	0
C	Druggable family + PDB, no drug	0
D	Druggable family + AlphaFold only, no drug	0
E	Difficult family or no structure, no drug	1	CCDC50

Undrugged target profiles

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

Symbol	ChEMBL assays	Drugged partners (top 3)
CCDC50	0	—

Clinical trials & evidence

Clinical trials

Clinical trials: 0.