Gene
SVBP
small vasohibin binding protein
- HGNC 29204↗(opens in a new tab)
- Ensembl gene ENSG00000177868↗(opens in a new tab)
- NCBI Gene 374969↗(opens in a new tab)
Summary
- Cytogenetic location
- 1p34.2
- Coordinates
- Chromosome 1: 42,807,052–42,817,397 (GRCh38)
- Exons
- 3 exons across 10.3 kb
- Protein
- 66 amino acids
- Also known as
- MGC45441
- Previous symbols
- CCDC23
- MANE Select transcript
- ENST00000372521.9NM_199342.4
- 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 SVBP yet. The test sequences your whole genome, so your data includes it all the same.
How SVBP 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 0.8 kb of the gene's 10.3 kb; 201 of those bases code for the protein.
How a genome test reads SVBP
3
positions in SVBP 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 10.3 kb of SVBP, introns included, not only the 0.8 kb of exons.
Traits linked to SVBP
The Human Phenotype Ontology lists these as features of the rare conditions SVBP can cause. Each trait's page lists the other genes linked to it.
Abnormality of limbs
- Intrinsic hand muscle atrophy
- Short 3rd toe
- Short 4th toe
- Short thumb
- Shortened 3rd long bone of hand
- Shortened 4th long bone of hand
- Shortened 5th long bone of hand
- Split hand
Show 2 more traits
Abnormality of the nervous system
- Delayed speech and language development
- Intellectual disability
- Epilepsy
- Hand mirror movements
- Motor delay
- Underdevelopment of part of brain called corpus callosum
- Autism spectrum disorder
- Dysplastic corpus callosum
Show 2 more traits
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.). SVBP gene: small vasohibin binding protein. Retrieved 16 October 2026, from https://dantelabs.com/genes/svbp
Dante Labs. SVBP gene: small vasohibin binding protein [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/svbp
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