Gene
IMPG1
interphotoreceptor matrix proteoglycan 1
- HGNC 6055↗(opens in a new tab)
- Ensembl gene ENSG00000112706↗(opens in a new tab)
- NCBI Gene 3617↗(opens in a new tab)
Summary
- Cytogenetic location
- 6q14.1
- Coordinates
- Chromosome 6: 75,921,114–76,072,662 (GRCh38)
- Exons
- 17 exons across 151.5 kb
- Protein
- 797 amino acids
- Also known as
- IPM150, GP147
- Previous symbols
- SPACR
- MANE Select transcript
- ENST00000369950.8NM_001563.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads IMPG1 yet. The test sequences your whole genome, so your data includes it all the same.
How IMPG1 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 3.5 kb of the gene's 151.5 kb; 2,394 of those bases code for the protein.
How a genome test reads IMPG1
14
positions in IMPG1 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 151.5 kb of IMPG1, introns included, not only the 3.5 kb of exons.
Traits linked to IMPG1
The Human Phenotype Ontology lists these as features of the rare conditions IMPG1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the eye
- Vitelliform macular lesion
- Abnormal electroretinogram
- Abnormal retinal pigmentation
- Abnormality of the eye
- Abnormality of vision
- Blindness
- Decreased Arden ratio of electrooculogram
- Extreme sensitivity of the eyes to light
Show 31 more traits
- Involuntary, rapid, rhythmic eye movements
- Optic atrophy
- Progressive night blindness
- Retina degeneration
- Spicular pigmentation of the retina
- Visual impairment
- Abnormal central response of multifocal electroretinogram
- Abnormal color vision
- Abnormal full-field electroretinogram
- Bulging cornea
- Chorioretinal scalloped atrophy
- Cystoid macular edema
- Difficulties with night vision
- Eye muscle paralysis
- Glaucoma
- Light eye color
- Loss of peripheral vision
- Moderate visual impairment
- Optic disc drusen
- Optic disc pallor
- Partial loss of field of vision
- Photoreceptor outer segment loss on macular OCT
- Posterior subcapsular cataract
- Retinal atrophy
- Decreased clarity of vision
- Photopsia
- Retinal nonattachment
- Color blindness
- Drusen
- Foveal hyperpigmentation
- Macular dystrophy
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.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). IMPG1 gene: interphotoreceptor matrix proteoglycan 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/impg1
Dante Labs. IMPG1 gene: interphotoreceptor matrix proteoglycan 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/impg1
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