Gene
FSD1L
fibronectin type III and SPRY domain containing 1 like
- HGNC 13753↗(opens in a new tab)
- Ensembl gene ENSG00000106701↗(opens in a new tab)
- NCBI Gene 83856↗(opens in a new tab)
Summary
- Cytogenetic location
- 9q31.2
- Coordinates
- Chromosome 9: 105,448,034–105,552,433 (GRCh38)
- Exons
- 14 exons across 104.4 kb
- Protein
- 530 amino acids
- Previous symbols
- CSDUFD1, CCDC10, FSD1NL, FSD1CL
- MANE Select transcript
- ENST00000481272.6NM_001145313.3
- 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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How FSD1L is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- 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 7.7 kb of the gene's 104.4 kb; 1,593 of those bases code for the protein.
Traits linked to FSD1L
The Human Phenotype Ontology lists these as features of the rare conditions FSD1L can cause. Each trait's page lists the other genes linked to it.
Abnormality of the eye
- Abnormal electroretinogram
- Cystoid macular edema
- Decreased clarity of vision
- Difficulties with night vision
- Hypoautofluorescent retinal lesion
- Limited peripheral vision
- Paracentral scotoma
- Perifoveal ring of hyperautofluorescence
Show 37 more traits
- Pseudophakia
- Retinal thinning
- Severe near sightedness
- Undetectable electroretinogram
- Abnormal retinal pigmentation
- Blindness
- Extreme sensitivity of the eyes to light
- 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
- Absent foveal reflex
- Blind spot located at fixation point
- Bulging cornea
- Close sighted
- Color blindness
- Cystoid macular degeneration
- Eye muscle paralysis
- Fundus hypopigmentation
- Glaucoma
- Loss of peripheral vision
- Macular atrophy
- Macular edema
- Optic disc drusen
- Optic disc pallor
- Photoreceptor outer segment loss on macular OCT
- Pigmentary retinopathy
- Posterior subcapsular cataract
- Progressive loss of vision
- Retinal atrophy
- Metamorphopsia
- Photopsia
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.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). FSD1L gene: fibronectin type III and SPRY domain containing 1 like. Retrieved 16 October 2026, from https://dantelabs.com/genes/fsd1l
Dante Labs. FSD1L gene: fibronectin type III and SPRY domain containing 1 like [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/fsd1l
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