Gene
HOMER2
homer scaffold protein 2
- HGNC 17513↗(opens in a new tab)
- Ensembl gene ENSG00000103942↗(opens in a new tab)
- NCBI Gene 9455↗(opens in a new tab)
Summary
- Cytogenetic location
- 15q25.2
- Coordinates
- Chromosome 15: 82,848,983–82,952,720 (GRCh38)
- Exons
- 9 exons across 103.7 kb
- Protein
- 343 amino acids
- Also known as
- CPD, Cupidin, Vesl-2, HOMER-2B, HOMER-2, HOMER-2A, DFNA68
- MANE Select transcript
- ENST00000450735.7NM_004839.4
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
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Hearing Loss and Deafness
- Autosomal Dominant Nonsyndromic Hearing LossAutosomal dominant
Autosomal dominant form of nonsyndromic deafness.
- 2 GenCC submitters rate it definitive or strong
- Nonsyndromic Genetic Hearing Loss
One of 97 genes linked to it
Inherited hearing loss without other medical features, including the common recessive forms caused by GJB2, OTOF, SLC26A4, STRC and many other genes, as well as dominant, X-linked and mitochondrial forms.
- ClinGen rates the link moderate
- 2 GenCC submitters rate it definitive or strong
▶Actionability
Knowing the genetic cause can guide hearing support and cochlear implant decisions, gene-therapy trial eligibility (for example OTOF) and family counselling.
How HOMER2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.9 kb of the gene's 103.7 kb; 1,032 of those bases code for the protein.
Sequencing HOMER2
2Low
How hard HOMER2 is to sequence with short reads, out of 100Each bar is the share of HOMER2's exon bases in that kind of difficult region. The score weighs them by how much each costs a short-read call: 0 when no base is in any, 100 when every base is in all of them.
- MappabilityStretches where 100 or 250 bp reads cannot be placed uniquely, so a call there may be missing or wrong. Weight 35%.0%
- HomologySegmental duplications: copies elsewhere in the genome, such as paralogues and pseudogenes, at 90% identity or more. Weight 30%.0%
- RepeatsTandem repeats and runs of one base, which reads slip on and may not span. Weight 15%.1.6%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. Weight 10%.13%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. Weight 10%.0%
2
positions in HOMER2 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 103.7 kb of HOMER2, introns included, not only the 1.9 kb of exons.
Genes linked to the same conditions
- ACTG1actin gamma 1Shares 2 conditions
- ATP11AATPase phospholipid transporting 11AShares 2 conditions
- ATP2B2ATPase plasma membrane Ca2+ transporting 2Shares 2 conditions
- CD164CD164 moleculeShares 2 conditions
- CEACAM16CEA cell adhesion molecule 16, tectorial membrane componentShares 2 conditions
- COCHcochlinShares 2 conditions
- COL11A1collagen type XI alpha 1 chainShares 2 conditions
- COL11A2collagen type XI alpha 2 chainShares 2 conditions
- DIAPH1diaphanous related formin 1Shares 2 conditions
- EYA4EYA transcriptional coactivator and phosphatase 4Shares 2 conditions
- GJB2gap junction protein beta 2Shares 2 conditions
- GJB6gap junction protein beta 6Shares 2 conditions
Traits linked to HOMER2
The Human Phenotype Ontology lists these as features of the rare conditions HOMER2 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-17: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
Cite this page
Dante Labs. (n.d.). HOMER2 gene: homer scaffold protein 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/homer2
Dante Labs. HOMER2 gene: homer scaffold protein 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/homer2
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