Gene
SEC24C
SEC24 homolog C, COPII component
- HGNC 10705↗(opens in a new tab)
- Ensembl gene ENSG00000176986↗(opens in a new tab)
- NCBI Gene 9632↗(opens in a new tab)
Summary
- Cytogenetic location
- 10q22.2
- Coordinates
- Chromosome 10: 73,744,372–73,772,161 (GRCh38)
- Exons
- 23 exons across 27.8 kb
- Protein
- 1,094 amino acids
- Also known as
- KIAA0079
- MANE Select transcript
- ENST00000345254.9NM_198597.3
- 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 SEC24C 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 4.4 kb of the gene's 27.8 kb; 3,285 of those bases code for the protein.
Traits linked to SEC24C
The Human Phenotype Ontology lists these as features of the rare conditions SEC24C can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormal facial shape
- Bulbous nose
- Cleft palate
- Corners of eye widely separated
- Eye folds
- Flattening of the skull base
- Prominent nasal bridge
- Upward slanting of the opening between the eyelids
Show 19 more traits
- Wide nasal bridge
- Abnormal dentition
- Abnormality of the eyelid
- Abnormality of the skull
- Dental cavities
- Long face
- Long philtrum
- Short neck
- Zygomatic flattening
- Abnormal tooth enamel
- Abnormally small head
- Blockage of the rear opening of the nasal cavity
- Downward slanting of the opening between the eyelids
- Little lower jaw
- Multiple suture craniosynostosis
- Narrow mouth
- Retinal arteriolar tortuosity
- Short philtrum
- Tall shaped head
Abnormality of the digestive system
- Anorectal anomaly
- Constipation
- Absent anus
- Acid reflux
- Enlarged colon lacking nerve cells
- Feeding difficulties in infancy
- Gallstones
- Inguinal hernia
Show 3 more traits
Abnormality of the eye
- Drooping upper eyelid
- New blood vessel formation in cornea
- Posterior embryotoxon
- Abnormally small eyeball
- Clouding of the lens of the eye
- Cross-eyed
- Glaucoma
- Optic atrophy
Show 1 more trait
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.). SEC24C gene: SEC24 homolog C, COPII component. Retrieved 17 October 2026, from https://dantelabs.com/genes/sec24c
Dante Labs. SEC24C gene: SEC24 homolog C, COPII component [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/sec24c
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